510(k) K062531 ยท NTE Temporary Carotid Catheter For Embolic Capture
ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE AND ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE
| Applicant | Cordis Corp., A Johnson & Johnson Co., Warren NJ, US |
| Decision | Substantially Equivalent, Sep 22, 2006 |
| Received | Aug 29, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062531
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.