The following data is part of a premarket notification filed by Bentley Laboratories, Inc. with the FDA for Cardiovascular Devices.
| Device ID | K820045 |
| 510k Number | K820045 |
| Device Name: | CARDIOVASCULAR DEVICES |
| 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 | 1982-01-07 |
| Decision Date | 1982-01-29 |