The following data is part of a premarket notification filed by Sorin Biomedical, Inc. with the FDA for Sorin Blood Cardioplegia System.
| Device ID | K934763 |
| 510k Number | K934763 |
| Device Name: | SORIN BLOOD CARDIOPLEGIA SYSTEM |
| Classification | Reservoir, Blood, Cardiopulmonary Bypass |
| Applicant | SORIN BIOMEDICAL, INC. 17600 GILLETTE AVE. P.O. BOX 19503 Irvine, CA 92713 -9503 |
| Contact | Terry Schultz |
| Correspondent | Terry Schultz SORIN BIOMEDICAL, INC. 17600 GILLETTE AVE. P.O. BOX 19503 Irvine, CA 92713 -9503 |
| Product Code | DTN |
| CFR Regulation Number | 870.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-10-05 |
| Decision Date | 1994-04-15 |