Cleared Traditional

K930074 - IN-VITRO DIAGNOSTIC REAGENT SET

K930074 is an FDA 510(k) clearance for IN-VITRO DIAGNOSTIC REAGENT SET, manufactured by Horizon Diagnostics, Inc.. The device is a Class 1 Chemistry device with product code JGJ cleared through the Traditional 510(k) pathway after a 124-day FDA review.

K930074 · Horizon Diagnostics, Inc. · Chemistry device
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May 1993
Decision
124d
Days
Class 1
Risk

K930074 is an FDA 510(k) clearance for the IN-VITRO DIAGNOSTIC REAGENT SET. Classified as Photometric Method, Magnesium (product code JGJ), Class I - General Controls.

Submitted by Horizon Diagnostics, Inc. (Jackson, US). The FDA issued a Cleared decision on May 11, 1993 after a review of 124 days - within the typical 510(k) review window.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1495 - 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 Horizon Diagnostics, Inc. devices

FDA 510(k) Submission Details - K930074

510(k) Number K930074 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 07, 1993
Decision Date May 11, 1993
Days to Decision 124 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
36d slower than avg
Panel avg: 88d · This submission: 124d
Pathway characteristics
Predicate-based equivalence.

JGJ Device Classification - Class 1, General Controls

Product Code JGJ Photometric Method, Magnesium
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1495
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - JGJ Photometric Method, Magnesium

All 84
Devices cleared under the same product code (JGJ) and FDA review panel - the closest regulatory comparables to K930074.
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