510(k) K943349 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
MAHURKAR DUAL LUMEN CATHETER
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Unknown, Mar 22, 1995 |
| Received | Jul 12, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943349
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.