510(k) K021272 ยท LKF Cannula, Manipulator/Injector, Uterine
SIB CATHETER, MODEL 61-7005
| Applicant | Ackrad Laboratories, Cranford NJ, US |
| Decision | Substantially Equivalent, May 21, 2002 |
| Received | Apr 22, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K021272
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.