The following data is part of a premarket notification filed by American Bentley with the FDA for Purges Lines, Pl-45 & Pl-33.
| Device ID | K833048 |
| 510k Number | K833048 |
| Device Name: | PURGES LINES, PL-45 & PL-33 |
| Classification | Filter, Blood, Cardiopulmonary Bypass, Arterial Line |
| Applicant | AMERICAN BENTLEY 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 | 1983-09-06 |
| Decision Date | 1983-10-20 |