510(k) K912660 ยท KMK Device, Intravascular Catheter Securement
SECURODRIP
| Applicant | Op-Co Medical Products , Ltd., New York NY, US |
| Decision | Substantially Equivalent, Dec 4, 1991 |
| Received | Jun 17, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912660
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.