510(k) K884259 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
MODIFIED LANDMARK VENOUS ACCESS DEVICE
| Applicant | Menlo Care, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Nov 1, 1988 |
| Received | Oct 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884259
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.