510(k) K891351 ยท KOH Instrument, Manual, General Obstetric-Gynecologic
NEWPORT LATERAL VAGINAL RETRACTOR
| Applicant | Simpson/Basye, Inc., Wilmington DE, US |
| Decision | Substantially Equivalent, May 11, 1989 |
| Received | Mar 10, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891351
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.