The following data is part of a premarket notification filed by Bentley Laboratories, Inc. with the FDA for Arterial Blood Filter Model #af-1040.
Device ID | K820343 |
510k Number | K820343 |
Device Name: | ARTERIAL BLOOD FILTER MODEL #AF-1040 |
Classification | Filter, Blood, Cardiopulmonary Bypass, Arterial Line |
Applicant | BENTLEY LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | DTM |
CFR Regulation Number | 870.4260 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-02-08 |
Decision Date | 1982-06-17 |