510(k) K974801 ยท HDP Elevator, Uterine
SINGLE CHANNEL BALLOON CANNULA
| Applicant | Conkin Surgical Instruments , Ltd., Toronta, Ontario, CA |
| Decision | Substantially Equivalent, Jul 9, 1998 |
| Received | Dec 22, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974801
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.