Cleared Traditional

K821200 - ALKALINE PHOSPHOTASE REAGENT SET

K821200 is the FDA 510(k) clearance for ALKALINE PHOSPHOTASE REAGENT SET by Omega Medical Electronics. It is a Class 2 Chemistry device (product code CIO) cleared through the Traditional 510(k) pathway after a 77-day FDA review.

K821200 · Omega Medical Electronics · Chemistry device
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Jul 1982
Decision
77d
Days
Class 2
Risk

K821200 is an FDA 510(k) clearance for the ALKALINE PHOSPHOTASE REAGENT SET. Classified as Thymolphthalein Monophosphate, Alkaline Phosphatase Or Isoenzymes (product code CIO), 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 862.1050 - 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 K821200 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 CIO Thymolphthalein Monophosphate, Alkaline Phosphatase Or Isoenzymes
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1050
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 - CIO Thymolphthalein Monophosphate, Alkaline Phosphatase Or Isoenzymes

Devices cleared under the same product code (CIO) and FDA review panel - the closest regulatory comparables to K821200.
ALKALINE PHOSPHATASE REAGENT SET
K860351 · Sterling Diagnostics, Inc. · Feb 1986
ALKALINE PHOSPHOTASE REAGENT SET
K841064 · Medical Specialties, Inc. · May 1984
COBAS STANDARDS FOR CALCIUM-IN-ORGANIC
K823578 · Hoffmann-La Roche, Inc. · Jan 1983
ALKALINE PHOSPHATASE TEST SET
K772257 · Stanbio Laboratory · Dec 1977
PHOSPHATASE PROCEDURE, TEKPOINT ALKALINE
K770453 · Icn Pharmaceuticals, Inc. · May 1977