510(k) K901300 ยท DWZ Device, Biopsy, Endomyocardial
BIOPSY FORCEPS
| Applicant | Portlyn Corp., Moultonboro NH, US |
| Decision | Substantially Equivalent, Jun 29, 1990 |
| Received | Mar 20, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901300
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.