510(k) K903732 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
KENDALL SAFETRAK(TM) HIGH FLOW CATHETER
| Applicant | Kendall Healthcare Products Co. Div.Of Tyco Health, Mansfield MA, US |
| Decision | Unknown, Oct 3, 1990 |
| Received | Aug 16, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903732
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.