510(k) K882242 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
LANDMARK(TM) VENOUS ACCESS DEVICE
| Applicant | Menlo Care, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Jun 20, 1988 |
| Received | May 20, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882242
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.