510(k) K092118 ยท DQO Catheter, Intravascular, Diagnostic
ANGIOGRAPHIC CATHETER, MODEL ANGIOS
| Applicant | Oscor, Inc., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Jan 13, 2010 |
| Received | Jul 14, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092118
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.