510(k) K871181 ยท HRX Arthroscope
ARTHROCOMBI 5003
| Applicant | F.M. Wiest USA, Inc., Cherry Hill NJ, US |
| Decision | Substantially Equivalent, Sep 29, 1987 |
| Received | Mar 25, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871181
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.