510(k) K021480 ยท FPA Set, Administration, Intravascular
EXTENSION SET LIGHT-SAFE, MODEL BC565
| Applicant | Codan US Corp., Santa Ana CA, US |
| Decision | Substantially Equivalent, Jun 27, 2002 |
| Received | May 8, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021480
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.