510(k) K912075 ยท KNA Instrument, Manual, Specialized Obstetric-Gynecologic
C-SECTION TRAY
| Applicant | Medical Device Inspection Co., Inc., Great Neck NY, US |
| Decision | Unknown, Apr 7, 1992 |
| Received | May 10, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912075
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.