510(k) K980212 ยท HDB Extractor, Vacuum, Fetal
MITYVAC
| Applicant | Prism Technologies, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jul 9, 1998 |
| Received | Jan 21, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980212
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.