Cleared Traditional

IN-VITRO DIAGNOSTIC REAGENT SET (K930074) - FDA 510(k) Clearance

Class I Chemistry device.

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

Submission Details

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.

Device Classification

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 89
Devices cleared under the same product code (JGJ) and FDA review panel - the closest regulatory comparables to K930074.
Magnesium
K181748 · Abbott Laboratories · Sep 2018
Magnesium
K173294 · Abbott Laboratories · May 2018
Randox RX Daytona Plus Magnesium (MG)
K162200 · Randox Laboratories, Ltd. · Apr 2017
Atellica CH Magnesium (Mg)
K162399 · Siemens Healthcare Diagnostics, Inc. · Jan 2017
MG
K981791 · Abbott Laboratories · Oct 1998
ROCHE DIAGNOSTICS MAGNESIUM REAGENT, CAT# 1551353
K983416 · Boehringer Mannheim Corp. · Oct 1998