510(k) K890751 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
ACCI-GUARD(TM) I.V. CATHETER PLACEMENT UNIT
| Applicant | Medical Safety Products, Inc., Denver CO, US |
| Decision | Substantially Equivalent, Apr 21, 1989 |
| Received | Feb 13, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890751
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.