K151254 is an FDA 510(k) clearance for the CARDIOSAVE Hybrid Intra-Aortic Balloon Pump. This device is classified as a System, Balloon, Intra-aortic And Control (Class II - Special Controls, product code DSP).
Submitted by Datascope Corp. (Manwah, US). The FDA issued a Cleared decision on July 2, 2015, 51 days after receiving the submission on May 12, 2015.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.3535.
| 510(k) Number | K151254 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 12, 2015 |
| Decision Date | July 02, 2015 |
| Days to Decision | 51 days |
| Submission Type | Special |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | DSP - System, Balloon, Intra-aortic And Control |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.3535 |