510(k) K982324 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
VECTRA PRO MODELS 2 AND 4
| Applicant | Chattanooga Group, Inc., Hixson TN, US |
| Decision | Substantially Equivalent, Feb 1, 1999 |
| Received | Jul 2, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982324
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.