510(k) K170726 ยท DWZ Device, Biopsy, Endomyocardial
Biopsy Forceps
| Applicant | Fehling Instruments GmbH & Co. KG, Karlstein, DE |
| Decision | Substantially Equivalent, Jun 2, 2017 |
| Received | Mar 9, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170726
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.