K960755 is an FDA 510(k) clearance for the CARDIOTHERM BLOOD CARDIOPLEGIA SYSTEMS. This device is classified as a Wire, Guide, Catheter (Class II - Special Controls, product code DQX).
Submitted by Medtronic Cardiac Surgery, Medtronic, Inc. (Anaheim, US). The FDA issued a Cleared decision on May 23, 1996, 90 days after receiving the submission on February 23, 1996.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.1330.
| 510(k) Number | K960755 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 23, 1996 |
| Decision Date | May 23, 1996 |
| Days to Decision | 90 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | DQX — Wire, Guide, Catheter |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.1330 |