510(k) K911747 ยท DQY Catheter, Percutaneous
PRO-GUIDE
| Applicant | American Interventional Technology, Lilburn GA, US |
| Decision | Substantially Equivalent, Sep 18, 1991 |
| Received | Apr 18, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911747
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.