510(k) K941098 ยท KMK Device, Intravascular Catheter Securement
SECURE-SITE
| Applicant | Op-Co Medical Products , Ltd., New York City NY, US |
| Decision | Substantially Equivalent, Aug 9, 1995 |
| Received | Mar 9, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941098
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.