510(k) K020890 ยท DQO Catheter, Intravascular, Diagnostic
SPYGLASS 4 FR ANGIOGRAPHICY CATHETER
| Applicant | St Jude Medical, Minnetonka MN, US |
| Decision | Substantially Equivalent, Apr 17, 2002 |
| Received | Mar 19, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020890
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.