510(k) K935822 ยท HCY Curette, Uterine
PHASE I CURETTE
| Applicant | Phase I Corp., Norwalk CT, US |
| Decision | Substantially Equivalent, Apr 28, 1994 |
| Received | Dec 3, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935822
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.