510(k) K921732 ยท KOH Instrument, Manual, General Obstetric-Gynecologic
MINOR LAP SET
| Applicant | Medikmark, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Jun 15, 1994 |
| Received | Apr 10, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921732
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.