510(k) K000632 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
0.9% SODIUM CHLORIDE VASCULAT ACCESS DEVICE
| Applicant | Avitro, LLC, Woodstock IL, US |
| Decision | Substantially Equivalent, Oct 19, 2000 |
| Received | Feb 24, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000632
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.