510(k) K973129 ยท KPM Shunt, Peritoneal
DENVER ASCITES SHUNTS, DENVER ASCITES SHUNT PERCUTANEOUS ACCESS KITS
| Applicant | Denver Biomaterials, Inc., Evergreen CO, US |
| Decision | Substantially Equivalent, Mar 17, 1998 |
| Received | Aug 21, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973129
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.