510(k) K882013 ยท DWO Needle, Biopsy, Cardiovascular
SOFT TISSUE BIOPSY DEVICE
| Applicant | Ocean Medical Products, Ltd., Wyoming MI, US |
| Decision | Substantially Equivalent, Jun 15, 1988 |
| Received | May 13, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882013
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.