The following data is part of a premarket notification filed by Supelco, Inc. with the FDA for Liquid Chromatography Columns.
Device ID | K894141 |
510k Number | K894141 |
Device Name: | LIQUID CHROMATOGRAPHY COLUMNS |
Classification | Columns, Liquid Chromatography |
Applicant | SUPELCO, INC. SUPELCO PARK Bellefonte, PA 16823 -0048 |
Contact | Lloyd Witting |
Correspondent | Lloyd Witting SUPELCO, INC. SUPELCO PARK Bellefonte, PA 16823 -0048 |
Product Code | DPM |
CFR Regulation Number | 862.2260 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-06-13 |
Decision Date | 1989-08-21 |