- Chattanooga Group Intelect Vet User Manual Online
- Chattanooga Intelect Legend Combo Manual
- Chattanooga Intelect Legend Xt Manual
- Chattanooga Intelect Legend Parts
Chattanooga Group Intelect Vet User Manual Online
View online Service manual for Chattanooga Group Vectra Genisys Medical Equipment or simply click Download button to examine the Chattanooga Group Vectra Genisys guidelines offline on your desktop or laptop computer. Chattanooga Group Intelect Vet, Chattanooga Group Intelect. Chattanooga Group Intelect Transport Combo User Manual. That Chattanooga Group pioneered 60 years ago, to the revolutionary advancements found in the Intelect Vet system, no other company knows physical therapy and rehabilitation like Chattanooga. Chattanooga is the world’s largest manufacturer of rehabilitation equipment for treating musculoskeletal, neurological and soft tissue disorders.
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Chattanooga Intelect Legend Combo Manual
| 510(k) | | | DeNovo | | | Registration & Listing | | | Adverse Events | | | Recalls | | | PMA | | | HDE | | | Classification | | | Standards |
| CFR Title 21 | | | Radiation-Emitting Products | | | X-Ray Assembler | | | Medsun Reports | | | CLIA | | | TPLC |
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Chattanooga Intelect Legend Xt Manual
Chattanooga Intelect Legend Parts
| New Search | Back to Search Results |
| | Class 2 Device Recall INTELECT VET |
| Date Initiated by Firm | December 17, 2007 |
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| Date Posted | June 25, 2008 |
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| Recall Status1 | Terminated 3 on February 19, 2010 |
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| Z-1223-2008 |
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| Recall Event ID | 46281 |
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| K031077 |
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Canine and equinine Muscle stimulator and therapeutic ultrasound - Product Code MPH
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| Product | INTELECT VET, Model No. 2756, Chattanooga Group, Hixson, TN 37343, Made in the USA |
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| Code Information | Serial numbers 1000 - 1140 |
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Recalling Firm/
Manufacturer | Chattanooga Corp Inc
4717 Adams Rd
Hixson TN 37343
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| For Additional Information Contact | Mr. Ben Whalen
423-648-4945 |
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| Device malfunction: causing electric shock and burn. |
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| Device Design |
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| Beginning on 12/17/2007, Chattanooga Corp. sent two recall notification letters, via UPS mail, to its consignees informing them of the situation. The letters stated that the recall was to the user level and requested that the user perform the software upgrade, which will eliminate the possibility of shock and burn. |
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| 140 units |
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| Worldwide Distribution - including USA |
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55. | | 510(K) Database | 510(K)s with Product Code = MPH and Original Applicant = CHATTANOOGA GROUP
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