510(k) K101651 ยท NTE Temporary Carotid Catheter For Embolic Capture
ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE
| Applicant | Cordis Corp., Bridgewater NJ, US |
| Decision | Substantially Equivalent, Jul 9, 2010 |
| Received | Jun 11, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101651
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.