The following data is part of a premarket notification filed by Supelco, Inc. with the FDA for Liquid Chromatography (hplc) Columns.
Device ID | K813575 |
510k Number | K813575 |
Device Name: | LIQUID CHROMATOGRAPHY (HPLC) 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 | 1981-12-23 |
Decision Date | 1982-01-18 |