510(k) K011862 ยท KPM Shunt, Peritoneal
DENVER ASCITES SHUNT AND PERCUTANEOUS ACCESS KIT WITH ASCITIES SHUNT
| Applicant | Denver Biomedical, Inc., Golden CO, US |
| Decision | Substantially Equivalent, Jul 12, 2001 |
| Received | Jun 14, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K011862
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.