510(k) K001694 ยท DQY Catheter, Percutaneous
GUIDANT RETRIEVER DEVICE
| Applicant | Guidant Cardiac and Vascular Surgery, Menlo Park CA, US |
| Decision | Substantially Equivalent, May 15, 2001 |
| Received | Jun 2, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001694
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.