510(k) K881412 ยท DWZ Device, Biopsy, Endomyocardial
MYOCARD BIOPSY FORCEP
| Applicant | Fehling Medizintechnik GmbH, West Germany, DE |
| Decision | Substantially Equivalent, Sep 8, 1988 |
| Received | Apr 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881412
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.