K962320 is an FDA 510(k) clearance for the S3 CARDIOPLEGIA CONTROL. This device is classified as a Heat-exchanger, Cardiopulmonary Bypass (Class II - Special Controls, product code DTR).
Submitted by Stoeckert Instrumente (North Attleboro, US). The FDA issued a Cleared decision on January 10, 1997, 207 days after receiving the submission on June 17, 1996.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.4240.
| 510(k) Number | K962320 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 17, 1996 |
| Decision Date | January 10, 1997 |
| Days to Decision | 207 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | Summary PDF |
| Product Code | DTR — Heat-exchanger, Cardiopulmonary Bypass |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.4240 |