510(k) K894371 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
NIPRO SAFELET CATH
| Applicant | Pharma-Plast USA, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Oct 25, 1989 |
| Received | Jul 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894371
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.