The following data is part of a premarket notification filed by Supelco, Inc. with the FDA for Capillary Gas Chromatographic Columns.
| Device ID | K841712 |
| 510k Number | K841712 |
| Device Name: | CAPILLARY GAS CHROMATOGRAPHIC COLUMNS |
| Classification | Columns, Glc |
| Applicant | SUPELCO, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DII |
| CFR Regulation Number | 862.2250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-04-24 |
| Decision Date | 1984-05-21 |