510(k) K865066 ยท HRX Arthroscope
ARTHROFLATOR
| Applicant | F.M. Wiest USA, Inc., Cherry Hill NJ, US |
| Decision | Substantially Equivalent, Apr 20, 1987 |
| Received | Dec 24, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K865066
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.