510(k) K922103 ยท KMK Device, Intravascular Catheter Securement
IAB ANCHOR
| Applicant | Datascope Corp., Oakland NJ, US |
| Decision | Substantially Equivalent, Aug 3, 1993 |
| Received | May 6, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922103
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.