510(k) K932010 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
V.A.D. ACCESS KIT
| Applicant | Clinipad Corp., Guilford CT, US |
| Decision | Substantially Equivalent, Feb 3, 1994 |
| Received | Apr 23, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932010
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.