FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MICROPROTEIN REAGENT SET

K Number: K921412 · Decision Jan 21, 1993
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
115
Applicant Total
41
Review Days
303

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Basic Information

Device Name
MICROPROTEIN REAGENT SET
K Number
K921412
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1635
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sterling Diagnostics, Inc.
Date Received
March 24, 1992
Decision Date
January 21, 1993
Product Code
CEK
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CEK Biuret (Colorimetric), Total Protein

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Other Clearances by Sterling Diagnostics, Inc.

K Number Device Name
K914609 TRIGLYCERIDES REAGENT SET
K914039 SODIUM REAGENT SET
K914040 PHOSPHOLIPID REAGENT SET
K862255 LACTATE DEHYDROGENASE (LDH) REAGENT SET (UV RATE)
K861962 VANILMANDELIC ACID (VMA) REAGENT SET
K862210 UREA NITROGEN (GLDH) REAGENT SET (UV)
K862256 ALKALINE PHOSPHATASE (PNPP RATE) REAGENT SET
K862209 ALT (SGPT) REAGENT SET (UV RATE)
K861855 HYDROXYBUTYRATE DEHYDROGENASE (HBD) REAGENT SET
K861713 SERUM POTASSIUM REAGENT SET
Search all 41 clearances from Sterling Diagnostics, Inc. →