510(k) K933235 ยท DWZ Device, Biopsy, Endomyocardial
CORDIS BIPAL 7 /BIOPSY & BIPAL BIOPSY FORCEPS, MODIF
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jan 6, 1994 |
| Received | May 19, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933235
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.