510(k) K910486 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
8 FR SINGLE LUMEN HIGH PERFORMANCE CATHETER
| Applicant | Davol, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Apr 19, 1991 |
| Received | Feb 6, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910486
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.