510(k) K950737 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
LANDMARK MIDLINE CATHETER
| Applicant | Menlo Care, Inc., Menlo Park CA, US |
| Decision | Substantially Equivalent, Mar 29, 1995 |
| Received | Feb 16, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950737
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.