510(k) K890665 ยท HRX Arthroscope
MODIFIED CANNULA, TROCAR AND OBTURATOR ACCESSORIES
| Applicant | Dyonics, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Nov 3, 1989 |
| Received | Feb 9, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890665
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.