The following data is part of a premarket notification filed by Delta Medical Industries with the FDA for L-3 Purge Line.
| Device ID | K802602 |
| 510k Number | K802602 |
| Device Name: | L-3 PURGE LINE |
| Classification | Filter, Blood, Cardiopulmonary Bypass, Arterial Line |
| Applicant | DELTA MEDICAL INDUSTRIES 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 | 1980-10-21 |
| Decision Date | 1980-11-12 |