510(k) K863337 ยท DQO Catheter, Intravascular, Diagnostic
CORDIPAK CARDIAC CATHETERIZATION PACK
| Applicant | Angi-Pak Corp., Miami FL, US |
| Decision | Substantially Equivalent, Sep 29, 1986 |
| Received | Aug 28, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863337
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.