The following data is part of a premarket notification filed by American Bentley with the FDA for Cardiotomy Reservoir Bcr-2000.
Device ID | K844366 |
510k Number | K844366 |
Device Name: | CARDIOTOMY RESERVOIR BCR-2000 |
Classification | Reservoir, Blood, Cardiopulmonary Bypass |
Applicant | AMERICAN BENTLEY 17502 ARMSTRONG AVE. Irvine, CA 92714 |
Contact | Donald A Raible |
Correspondent | Donald A Raible AMERICAN BENTLEY 17502 ARMSTRONG AVE. Irvine, CA 92714 |
Product Code | DTN |
CFR Regulation Number | 870.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-11-13 |
Decision Date | 1985-01-14 |