510(k) K010349 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
DUAL LUMEN MIDLINE CATHETER
| Applicant | Catheter Innovations, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Feb 28, 2001 |
| Received | Feb 5, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K010349
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.