510(k) K134031 ยท LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous
THREADER MONORAIL MICRO-DILATATION CATHETER, THREADER OVER-THE-WIRE MICRO-DILATATION CATHETER
| Applicant | Boston Scientific Corporation, Maple Grove MN, US |
| Decision | Substantially Equivalent, Jul 21, 2014 |
| Received | Dec 31, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K134031
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.