510(k) K933638 ยท HRX Arthroscope
ACUMED CARPAL TUNNEL RELEASE KIT
| Applicant | Acu Med, Inc., Beaverton OR, US |
| Decision | Substantially Equivalent, Mar 24, 1994 |
| Received | Jul 27, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933638
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.