510(k) K897070 ยท HFE Brush, Endometrial
ENDOBRUSH(TM) DEVICE; OMNIBRUSH
| Applicant | Intl. Cytobrush, Inc., Hollywood FL, US |
| Decision | Substantially Equivalent, Sep 10, 1990 |
| Received | Dec 22, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K897070
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.