510(k) K980237 ยท KNA Instrument, Manual, Specialized Obstetric-Gynecologic
GYNEX ENDOSPECULUM
| Applicant | Gynex Corp., Concord CA, US |
| Decision | Substantially Equivalent, Apr 8, 1998 |
| Received | Jan 23, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980237
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.