510(k) K770751 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
CATHETERS, OVER-THE-NEEDLE
| Applicant | Cutter Laboratories, Inc., Walker MI, US |
| Decision | Substantially Equivalent, May 26, 1977 |
| Received | Apr 25, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770751
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.