510(k) K903620 ยท HRX Arthroscope
MODIFIED ENDOSCOPIC CARPAL TUNNEL RELEASE SYSTEM
| Applicant | Smith & Nephew Dyonics, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Oct 12, 1990 |
| Received | Aug 7, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903620
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.