510(k) K112797 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER
| Applicant | Cordis Corp., Bridgewater NJ, US |
| Decision | Substantially Equivalent, May 4, 2012 |
| Received | Sep 26, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112797
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.