510(k) K870186 ยท DWZ Device, Biopsy, Endomyocardial
ENDOMYOCARDIAL BIOPSY DEVICE
| Applicant | Mansfield Scientific, Inc., Mansfield MA, US |
| Decision | Substantially Equivalent, Feb 20, 1987 |
| Received | Jan 16, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870186
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.