510(k) K912165 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
LANDMARK DUAL-LUMEN MIDLINE CATHETER SYSTEM
| Applicant | Menlo Care, Inc., Menlo Park CA, US |
| Decision | Unknown, Dec 11, 1991 |
| Received | May 16, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912165
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.