K093965 is an FDA 510(k) clearance for the ULTRAVERSE 014 AND 018 BALLOON DILATATION CATHETERS. This device is classified as a Catheter, Angioplasty, Peripheral, Transluminal (Class II - Special Controls, product code LIT).
Submitted by C.R. Bard, Inc. (Tempe, US). The FDA issued a Cleared decision on March 17, 2010, 84 days after receiving the submission on December 23, 2009.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1250.
| 510(k) Number | K093965 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 23, 2009 |
| Decision Date | March 17, 2010 |
| Days to Decision | 84 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | LIT — Catheter, Angioplasty, Peripheral, Transluminal |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1250 |