510(k) K973818 ยท DWZ Device, Biopsy, Endomyocardial
T-REX BIOPSY FORCEPS
| Applicant | Boston Scientific Corp, Redmond WA, US |
| Decision | Substantially Equivalent, Dec 16, 1997 |
| Received | Oct 7, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973818
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.