510(k) K111899 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
ARMADA 35/35LL PTA CATHETER
| Applicant | Abbott Vascular, Santa Clara CA, US |
| Decision | Substantially Equivalent, Oct 3, 2011 |
| Received | Jul 5, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111899
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 25, 2012 | Abbott Vascular Armada 35/ Armada 35 LL PTA Catheters. The device is intended for dilatation of lesions in the vasculature. Terminated |
LIT | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.