510(k) K000409 ยท DWZ Device, Biopsy, Endomyocardial
MODIFICATION TO T-REX BIOPSY FORCEPS
| Applicant | Boston Scientific Corp, Redmond WA, US |
| Decision | Substantially Equivalent, Feb 28, 2000 |
| Received | Feb 8, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K000409
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.