510(k) K921902 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
PORT ACCESS NEEDLE
| Applicant | Kawasumi Laboratories Co., Ltd., Tokyo, JP |
| Decision | Substantially Equivalent, Jul 28, 1993 |
| Received | Apr 22, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921902
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.