510(k) K003451 ยท KPM Shunt, Peritoneal
DENVER PAK W/ DOUBLE-VALVE ASCITES SHUNT,DENVER PAK W/ SINGLE-VALVED ASCITES SHUNT, DENVER PAK, DOUBLED-VALVED ASCITES T
| Applicant | Denver Biomedicals, Inc., Golden CO, US |
| Decision | Substantially Equivalent, Jan 2, 2001 |
| Received | Nov 7, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K003451
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.