Cleared Traditional

K121364 - SHIGA TOXIN QUIK CHEK

K121364 is an FDA 510(k) clearance for SHIGA TOXIN QUIK CHEK, manufactured by Techlab Inc., Corporate Research Center. The device is a Class 1 Microbiology device with product code GMZ cleared through the Traditional 510(k) pathway after a 148-day FDA review.

K121364 · Techlab Inc., Corporate Research Center · Microbiology device
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Oct 2012
Decision
148d
Days
Class 1
Risk

K121364 is an FDA 510(k) clearance for the SHIGA TOXIN QUIK CHEK. Classified as Antigens, All Types, Escherichia Coli (product code GMZ), Class I - General Controls.

Submitted by Techlab Inc., Corporate Research Center (Blacksburg, US). The FDA issued a Cleared decision on October 2, 2012 after a review of 148 days - within the typical 510(k) review window.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.3255 - the FDA microbiology device 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 Microbiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Techlab Inc., Corporate Research Center devices

FDA 510(k) Submission Details - K121364

510(k) Number K121364 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 07, 2012
Decision Date October 02, 2012
Days to Decision 148 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
46d slower than avg
Panel avg: 102d · This submission: 148d
Pathway characteristics
Predicate-based equivalence.

GMZ Device Classification - Class 1, General Controls

Product Code GMZ Antigens, All Types, Escherichia Coli
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.3255
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 - GMZ Antigens, All Types, Escherichia Coli

All 10
Devices cleared under the same product code (GMZ) and FDA review panel - the closest regulatory comparables to K121364.
Curian® Shiga Toxin
K222829 · Meridian Bioscience, Inc. · Apr 2023
SHIGA TOXIN CHEK
K121411 · Techlab Inc., Corporate Research Center · Oct 2012
IMMUNOCARD STAT! EHEC, MODEL 751630
K062546 · Meridian Bioscience, Inc. · Feb 2007
IMMUNOCARD STAT! E. COLI O157 PLUS
K023599 · Meridian Bioscience, Inc. · Jan 2003
IMMUNOCARD STAT! E. COLI O157:H7
K990263 · Meridian Diagnostics, Inc. · Aug 1999
PROSPECT SHIGA TOXIN MICROPLATE ASSAY
K980507 · Alexon - Trend, Inc. · Apr 1998