Cleared Special

K132352 - SAS FLUALERT A & B

K132352 is the FDA 510(k) clearance for SAS FLUALERT A & B by Sa Scientific , Ltd.. It is a Class 1 Microbiology device (product code GNX) cleared through the Special 510(k) pathway after a 24-day FDA review.

K132352 · Sa Scientific , Ltd. · Microbiology device
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Aug 2013
Decision
24d
Days
Class 1
Risk

K132352 is an FDA 510(k) clearance for the SAS FLUALERT A & B, SAS INFLUENZA A TEST. Classified as Antigens, Cf (including Cf Control), Influenza Virus A, B, C (product code GNX), Class I - General Controls.

Submitted by Sa Scientific , Ltd. (San Antonio, US). The FDA issued a Cleared decision on August 22, 2013 after a review of 24 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.3330 - the FDA microbiology device framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Sa Scientific , Ltd. devices

Submission Details

510(k) Number K132352 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 29, 2013
Decision Date August 22, 2013
Days to Decision 24 days
Submission Type Special
Review Panel Microbiology (MI)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
78d faster than avg
Panel avg: 102d · This submission: 24d
Pathway characteristics
Modification to existing cleared device.

Device Classification

Product Code GNX Antigens, Cf (including Cf Control), Influenza Virus A, B, C
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 866.3330
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 - GNX Antigens, Cf (including Cf Control), Influenza Virus A, B, C

Devices cleared under the same product code (GNX) and FDA review panel - the closest regulatory comparables to K132352.
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