Cleared Traditional

K922490 - ABBOTT STREP A CONTROLS

K922490 is an FDA 510(k) clearance for ABBOTT STREP A CONTROLS, manufactured by Abbott Laboratories. The device is a Class 1 Microbiology device with product code GTY cleared through the Traditional 510(k) pathway after a 56-day FDA review.

K922490 · Abbott Laboratories · Microbiology device
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Jul 1992
Decision
56d
Days
Class 1
Risk

K922490 is an FDA 510(k) clearance for the ABBOTT STREP A CONTROLS. Classified as Antigens, All Groups, Streptococcus Spp. (product code GTY), Class I - General Controls.

Submitted by Abbott Laboratories (Abbott Park, US). The FDA issued a Cleared decision on July 22, 1992 after a review of 56 days - a notably fast clearance cycle.

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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Abbott Laboratories devices

FDA 510(k) Submission Details - K922490

510(k) Number K922490 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 27, 1992
Decision Date July 22, 1992
Days to Decision 56 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
46d faster than avg
Panel avg: 102d · This submission: 56d
Pathway characteristics
Predicate-based equivalence.

GTY Device Classification - Class 1, General Controls

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 34
Devices cleared under the same product code (GTY) and FDA review panel - the closest regulatory comparables to K922490.
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