510(k) K921412

MICROPROTEIN REAGENT SET by Sterling Diagnostics, Inc. — Product Code CEK

K921412 is an FDA 510(k) premarket notification submitted by Sterling Diagnostics, Inc. for the device "MICROPROTEIN REAGENT SET". The FDA issued a decision of Substantially Equivalent on January 21, 1993. The device falls under product code CEK (Biuret (Colorimetric), Total Protein), a Class II device regulated under 21 CFR 862.1635. Sterling Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 21, 1993
Date Received
March 24, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Biuret (Colorimetric), Total Protein
Device Class
Class II
Regulation Number
862.1635
Review Panel
CH
Submission Type