510(k) K960549 ยท HDB Extractor, Vacuum, Fetal
MITYVAC DIRECTIONAL VACUUM EXTRACTOR, DISPOSABLE
| Applicant | Neward Enterprises, Inc., Cucamonga CA, US |
| Decision | Substantially Equivalent, Aug 29, 1996 |
| Received | Feb 8, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960549
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.