510(k) K001874 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
PERIPHERALLY INSERTED CENTRAL CATHETER
| Applicant | Utah Medical Products, Inc., Midvale UT, US |
| Decision | Substantially Equivalent, Sep 25, 2000 |
| Received | Jun 20, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001874
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.