510(k) K935514 ยท FMI Needle, Hypodermic, Single Lumen
VACUUM TUBE HOLDER CULTURE MEDIUM VIAL HOLDER
| Applicant | Kawasumi Laboratories Co., Ltd., Tokyo, JP |
| Decision | Substantially Equivalent, Feb 10, 1994 |
| Received | Nov 16, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935514
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.