510(k) K910840 ยท DWZ Device, Biopsy, Endomyocardial
VASCULAR BIOPSY FORCEPS
| Applicant | Vascular Products, Inc., Tarpon Springs FL, US |
| Decision | Substantially Equivalent, Jul 15, 1991 |
| Received | Feb 27, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910840
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.