510(k) K880570 ยท KPM Shunt, Peritoneal
DENVER PLEURO-PERITONEAL SHUNT
| Applicant | Codman & Shurtleff, Inc., Randolph MA, US |
| Decision | Substantially Equivalent, Jun 20, 1988 |
| Received | Feb 10, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880570
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.