510(k) K992051 ยท DQO Catheter, Intravascular, Diagnostic
RADIFOCUS OPTITORQUE
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Aug 10, 1999 |
| Received | Jun 18, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K992051
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.