K792152 is an FDA 510(k) clearance for the CARDIOPLEGIA SOLUTION ADMIN. SET. This device is classified as a Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass (Class II - Special Controls, product code DWF).
Submitted by Cardio Systems, Inc. (Mchenry, US). The FDA issued a Cleared decision on November 13, 1979, 22 days after receiving the submission on October 22, 1979.
This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.4210.
| 510(k) Number | K792152 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 22, 1979 |
| Decision Date | November 13, 1979 |
| Days to Decision | 22 days |
| Submission Type | Traditional |
| Review Panel | Cardiovascular (CV) |
| Summary | — |
| Product Code | DWF — Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 870.4210 |