The following data is part of a premarket notification filed by American Bentley with the FDA for Arterial/venous Sample Line Bos-cmsl.
Device ID | K853950 |
510k Number | K853950 |
Device Name: | ARTERIAL/VENOUS SAMPLE LINE BOS-CMSL |
Classification | Adaptor, Stopcock, Manifold, Fitting, 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 | DTL |
CFR Regulation Number | 870.4290 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-09-25 |
Decision Date | 1985-12-11 |