510(k) K880401 ยท KPM Shunt, Peritoneal
DENVER PERITONEO-VENOUS SHUNT
| Applicant | Codman & Shurtleff, Inc., Randolph MA, US |
| Decision | Substantially Equivalent, May 31, 1988 |
| Received | Jan 29, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880401
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.