510(k) K952852 ยท FPA Set, Administration, Intravascular
NIMA (NEEDLELESS INJECTIONSITE MASTER ADAPTER) & I.V. SET
| Applicant | Critical Device Corp., Brea CA, US |
| Decision | Substantially Equivalent, Feb 16, 1996 |
| Received | Jun 21, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952852
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.