The following data is part of a premarket notification filed by Bentley Laboratories, Inc. with the FDA for Blood Oxygenators #bos-105s Bos-5s W/.
Device ID | K822803 |
510k Number | K822803 |
Device Name: | BLOOD OXYGENATORS #BOS-105S BOS-5S W/ |
Classification | Oxygenator, Cardiopulmonary Bypass |
Applicant | BENTLEY LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | DTZ |
CFR Regulation Number | 870.4350 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-09-17 |
Decision Date | 1982-11-01 |