510(k) K890453 ยท DWZ Device, Biopsy, Endomyocardial
REUSABLE MLYOCARDIAL BIOPSY FORCEPS (BIOPTOMES
| Applicant | Dlp, Inc., Grand Rapids MI, US |
| Decision | Substantially Equivalent, Mar 31, 1989 |
| Received | Jan 30, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890453
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.