510(k) K172494 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
PROTEUS PTA Balloon Catheter with Embolic Capture Feature
| Applicant | Angioslide, Ltd., Netanya, IL |
| Decision | Substantially Equivalent, Dec 15, 2017 |
| Received | Aug 18, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K172494
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.