510(k) K912798 ยท DQX Wire, Guide, Catheter
AMPLANTZ AND BENTSON GUIDEWIRES
| Applicant | Meadox Medicals, Div. Boston Scientific Corp., Oakland NJ, US |
| Decision | Substantially Equivalent, Sep 23, 1991 |
| Received | Jun 25, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912798
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.