510(k) K913397 ยท DQO Catheter, Intravascular, Diagnostic
MEGA ANGIOGRAM KIT
| Applicant | Mega Medical, Inc., Tampa FL, US |
| Decision | Unknown, Oct 31, 1991 |
| Received | Jul 30, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913397
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.