Cleared Traditional

K023766 - ACON STREP A TWIST TEST DEVICE

K023766 is the FDA 510(k) clearance for ACON STREP A TWIST TEST DEVICE by Acon Laboratories Co.. It is a Class 1 Microbiology device (product code GTY) cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K023766 · Acon Laboratories Co. · Microbiology device
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Feb 2003
Decision
90d
Days
Class 1
Risk

K023766 is an FDA 510(k) clearance for the ACON STREP A TWIST TEST DEVICE. Classified as Antigens, All Groups, Streptococcus Spp. (product code GTY), Class I - General Controls.

Submitted by Acon Laboratories Co. (San Diego, US). The FDA issued a Cleared decision on February 10, 2003 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.3740 - 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 Acon Laboratories Co. devices

Submission Details

510(k) Number K023766 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 12, 2002
Decision Date February 10, 2003
Days to Decision 90 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
12d faster than avg
Panel avg: 102d · This submission: 90d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code GTY Antigens, All Groups, Streptococcus Spp.
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.3740
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 - GTY Antigens, All Groups, Streptococcus Spp.

All 29
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SAS STREPALERT
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