Cleared Traditional

K912027 - CALCIUM (ARSENAZO III) REAGENT, UNIVERSAL

K912027 is an FDA 510(k) clearance for CALCIUM (ARSENAZO III) REAGENT, manufactured by Enzyme Technology, Inc.. The device is a Class 2 Chemistry device with product code CIC cleared through the Traditional 510(k) pathway after a 267-day FDA review.

K912027 · Enzyme Technology, Inc. · Chemistry device
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Jan 1992
Decision
267d
Days
Class 2
Risk

K912027 is an FDA 510(k) clearance for the CALCIUM (ARSENAZO III) REAGENT, UNIVERSAL. Classified as Cresolphthalein Complexone, Calcium (product code CIC), Class II - Special Controls.

Submitted by Enzyme Technology, Inc. (Shelton, US). The FDA issued a Cleared decision on January 30, 1992 after a review of 267 days - an extended review cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1145 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Chemistry review framework, consistent with the majority of Class II 510(k) submissions.

View all Enzyme Technology, Inc. devices

FDA 510(k) Submission Details - K912027

510(k) Number K912027 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 08, 1991
Decision Date January 30, 1992
Days to Decision 267 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
179d slower than avg
Panel avg: 88d · This submission: 267d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CIC Device Classification - Class 2, Special Controls

Product Code CIC Cresolphthalein Complexone, Calcium
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1145
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 - CIC Cresolphthalein Complexone, Calcium

All 90
Devices cleared under the same product code (CIC) and FDA review panel - the closest regulatory comparables to K912027.
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