510(k) K946082 ยท FPA Set, Administration, Intravascular
BEECH PRO LOK FIXED
| Applicant | Beech Medical Products, Inc., Middlesex NJ, US |
| Decision | Substantially Equivalent, Mar 13, 1995 |
| Received | Dec 13, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K946082
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.