510(k) K151141 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
Cronus HP - High Pressure Peripheral Balloon Catheter
| Applicant | Nipro Medical Corporation, Miami FL, US |
| Decision | Substantially Equivalent, Jan 14, 2016 |
| Received | Apr 29, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151141
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.