510(k) K102633 ยท DQO Catheter, Intravascular, Diagnostic
BIOTEQ ANGIOGRAPHIC CATHETER
| Applicant | Bioteque Corp., Flagstaff AZ, US |
| Decision | Substantially Equivalent, Sep 9, 2011 |
| Received | Sep 13, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102633
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.