The following data is part of a premarket notification filed by Supelco, Inc. with the FDA for Liquid Chromatography Columns.
| Device ID | K802703 |
| 510k Number | K802703 |
| Device Name: | LIQUID CHROMATOGRAPHY COLUMNS |
| Classification | Columns, Liquid Chromatography |
| Applicant | SUPELCO, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DPM |
| CFR Regulation Number | 862.2260 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-10-31 |
| Decision Date | 1980-11-12 |