510(k) K000620 ยท MDG System, Intrafallopian Cannula
PBN FALLOPIAN TUBE CATHETER SYSTEM
| Applicant | Medical Device Technologies, Inc., Gainesville FL, US |
| Decision | Substantially Equivalent, Oct 30, 2000 |
| Received | Feb 24, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000620
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.