510(k) K870897 ยท FFO Retractor, Self-Retaining
KODNER ANAL PERIONEAL RETRACTOR
| Applicant | Sur-Med Instruments, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Jun 4, 1987 |
| Received | Mar 5, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870897
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.