510(k) K041094 ยท LKF Cannula, Manipulator/Injector, Uterine
HSG CATHETER SET
| Applicant | Bioteque America, Inc., Langhorne PA, US |
| Decision | Substantially Equivalent, Jun 17, 2004 |
| Received | Apr 27, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041094
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.