Cleared Traditional

K821210 - SERUM TOTAL PROTEIN REAGENT SET

K821210 is the FDA 510(k) clearance for SERUM TOTAL PROTEIN REAGENT SET by Omega Medical Electronics. It is a Class 2 Chemistry device (product code CEK) cleared through the Traditional 510(k) pathway after a 77-day FDA review.

K821210 · Omega Medical Electronics · Chemistry device
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Jul 1982
Decision
77d
Days
Class 2
Risk

K821210 is an FDA 510(k) clearance for the SERUM TOTAL PROTEIN REAGENT SET. Classified as Biuret (colorimetric), Total Protein (product code CEK), Class II - Special Controls.

Submitted by Omega Medical Electronics (Mchenry, US). The FDA issued a Cleared decision on July 13, 1982 after a review of 77 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1635 - the FDA in vitro diagnostics and chemistry framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Omega Medical Electronics devices

Submission Details

510(k) Number K821210 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 27, 1982
Decision Date July 13, 1982
Days to Decision 77 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
11d faster than avg
Panel avg: 88d · This submission: 77d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code CEK Biuret (colorimetric), Total Protein
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1635
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - CEK Biuret (colorimetric), Total Protein

All 80
Devices cleared under the same product code (CEK) and FDA review panel - the closest regulatory comparables to K821210.
LIQUIZYME TOTAL PROTEIN REAGENT
K823170 · Amresco, Inc. · Nov 1982
PSI TOTAL PROTEIN REAGENT
K822468 · Pointe Scientific, Inc., · Sep 1982
BIURET (COLORIMETRIC) TOTAL PROTEIN
K821905 · American Monitor Corp. · Jul 1982
RA-1000 SYSTEM ADD'L ANALYTES PHASE III
K820913 · Technicon Instruments Corp. · May 1982
ASTRA TOTAL PROTEIN REAGENT
K813536 · Hi Chem, Inc. · Dec 1981
ULTRACHEM TP, ITEM #64974
K813038 · Harleco · Nov 1981