510(k) K813345 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
CRITIKON I.V. CATHETER PLACEMENT UNIT
| Applicant | Critikon Company, LLC, Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 12, 1982 |
| Received | Nov 25, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813345
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.