510(k) K020954 ยท LKF Cannula, Manipulator/Injector, Uterine
H/S PROCEDURE TRAY (5F), H/S PROCEDURE TRAY (7F), H/S ELLIPTOSPHERE PROCEDURE TRAY & MULTIPURPOSE PROCEDURE TRAY
| Applicant | Ackrad Laboratories, Cranford NJ, US |
| Decision | Substantially Equivalent, Apr 24, 2002 |
| Received | Mar 25, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020954
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.