510(k) K896046 ยท KMK Device, Intravascular Catheter Securement
VITAPATCH CATH. SECUREMENT DEVICE W/CHLORHEXIDINE
| Applicant | Vitaphore Corp., Menlo Park CA, US |
| Decision | Substantially Equivalent, Jan 11, 1990 |
| Received | Oct 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896046
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.