510(k) K792631 ยท KNA Instrument, Manual, Specialized Obstetric-Gynecologic
STERILIZATION PROCESS/DBL. GRIP CORD CLP
| Applicant | Procter & Gamble Mfg. Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 28, 1980 |
| Received | Dec 19, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792631
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.