510(k) K981382 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
PASV DUAL LUMEN PERIPHERALLY INSERTED MIDLINE CATHETER MODEL NUMBER MIDLINE-NUMEROUS
| Applicant | Catheter Innovations, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, May 1, 1998 |
| Received | Apr 16, 1998 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K981382
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.