510(k) K921755 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
8 FR SINGLE LUMEN HIGH PERF. GROSHONG CENT. VENOUS
| Applicant | Davol, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Oct 23, 1992 |
| Received | Apr 13, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921755
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.