K093969 is an FDA 510(k) clearance for the ACUITY BREAK-AWAY GUIDE CATHETER. This device is classified as a Catheter, Percutaneous (Class II - Special Controls, product code DQY).
Submitted by Cardiac Pacemakers, Inc. (St. Paul, US). The FDA issued a Cleared decision on March 5, 2010, 72 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 | K093969 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 23, 2009 |
| Decision Date | March 05, 2010 |
| Days to Decision | 72 days |
| Submission Type | Special |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | DQY — Catheter, Percutaneous |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1250 |