510(k) K933852 ยท FPA Set, Administration, Intravascular
PRO-LOK EXTENSION SET
| Applicant | Beech Medical Products, Inc., Newtown PA, US |
| Decision | Substantially Equivalent, Dec 29, 1993 |
| Received | Aug 6, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933852
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.