K112452 is an FDA 510(k) clearance for the ANGIODYNAMICS SOFT-VU ANGIOGRAPHIC CATHETERS. This device is classified as a Catheter, Intravascular, Diagnostic (Class II - Special Controls, product code DQO).
Submitted by AngioDynamics, Inc. (Latham, US). The FDA issued a Cleared decision on March 30, 2012, 218 days after receiving the submission on August 25, 2011.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1200.
| 510(k) Number | K112452 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 25, 2011 |
| Decision Date | March 30, 2012 |
| Days to Decision | 218 days |
| Submission Type | Special |
| Review Panel | Cardiovascular (CV) |
| Summary | Statement |
| Product Code | DQO — Catheter, Intravascular, Diagnostic |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1200 |