510(k) K964812 ยท FPA Set, Administration, Intravascular
NIMA NEEDLELESS INJECTIONSITE MASTER ADAPTER AND I.V. SET
| Applicant | Critical Device Corp., Brea CA, US |
| Decision | Substantially Equivalent, Feb 10, 1997 |
| Received | Nov 29, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964812
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.