510(k) K984482 ยท DQY Catheter, Percutaneous
AVE GL-1 GUIDING CATHETER
| Applicant | Arterial Vascular Engineering Massachusetts, Inc., Billerica MA, US |
| Decision | Substantially Equivalent, Jul 30, 1999 |
| Received | Dec 16, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984482
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.