510(k) K953034 ยท LKF Cannula, Manipulator/Injector, Uterine
H/S CATHETER SET(61-3005, 61-3007, 61-3605, 61-3607)
| Applicant | Ackrad Laboratories, Cranford NJ, US |
| Decision | Substantially Equivalent, Aug 29, 1995 |
| Received | Jun 19, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953034
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.