510(k) K953300 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
V-CATH DUAL LUMEN E.S.P. PERIPHERAL INSERTED CENTRAL CATHETER
| Applicant | Hdc Corp., San Jose CA, US |
| Decision | Substantially Equivalent, Apr 30, 1996 |
| Received | Jul 14, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953300
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.