The following data is part of a premarket notification filed by Shiley, Inc. with the FDA for Bcd Advanced.
| Device ID | K910923 |
| 510k Number | K910923 |
| Device Name: | BCD ADVANCED |
| Classification | Heat-exchanger, Cardiopulmonary Bypass |
| Applicant | SHILEY, INC. 17600 GILLETTE AVE. P.O. BOX 19503 Irvine, CA 92714 |
| Contact | Allan Abati |
| Correspondent | Allan Abati SHILEY, INC. 17600 GILLETTE AVE. P.O. BOX 19503 Irvine, CA 92714 |
| Product Code | DTR |
| CFR Regulation Number | 870.4240 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-03-05 |
| Decision Date | 1991-04-09 |