The following data is part of a premarket notification filed by Sterling Diagnostics, Inc. with the FDA for Microprotein Reagent Set.
Device ID | K921412 |
510k Number | K921412 |
Device Name: | MICROPROTEIN REAGENT SET |
Classification | Biuret (colorimetric), Total Protein |
Applicant | STERLING DIAGNOSTICS, INC. 6226 PRODUCT DR. Sterling Heights, MI 48312 |
Contact | David L Callender |
Correspondent | David L Callender STERLING DIAGNOSTICS, INC. 6226 PRODUCT DR. Sterling Heights, MI 48312 |
Product Code | CEK |
CFR Regulation Number | 862.1635 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-03-24 |
Decision Date | 1993-01-21 |