Cleared Traditional

K052439 - AESKULISA GLIA A AND AESKULISA GLIA G

K052439 is an FDA 510(k) clearance for AESKULISA GLIA A AND AESKULISA GLIA G, manufactured by Aesku Diagnostics. The device is a Class 2 Immunology device with product code MST cleared through the Traditional 510(k) pathway after a 154-day FDA review.

K052439 · Aesku Diagnostics · Immunology device
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Feb 2006
Decision
154d
Days
Class 2
Risk

K052439 is an FDA 510(k) clearance for the AESKULISA GLIA A AND AESKULISA GLIA G. Classified as Antibodies, Gliadin (product code MST), Class II - Special Controls.

Submitted by Aesku Diagnostics (Miami, US). The FDA issued a Cleared decision on February 7, 2006 after a review of 154 days - an extended review cycle.

This device falls under the Immunology FDA review panel, regulated under 21 CFR 866.5750 - the FDA immunology 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 Immunology review framework, consistent with the majority of Class II 510(k) submissions.

View all Aesku Diagnostics devices

FDA 510(k) Submission Details - K052439

510(k) Number K052439 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 06, 2005
Decision Date February 07, 2006
Days to Decision 154 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
50d slower than avg
Panel avg: 104d · This submission: 154d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MST Device Classification - Class 2, Special Controls

Product Code MST Antibodies, Gliadin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.5750
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Immunology devices follow this clearance model.

Regulatory Peers - MST Antibodies, Gliadin

All 29
Devices cleared under the same product code (MST) and FDA review panel - the closest regulatory comparables to K052439.
ELIA GLIADIN IGA, IGG AND CELIAC CONTROL
K063775 · Phadia US, Inc. · Mar 2007
QUANTA LITE H-TTG/DGP SCREEN
K070083 · Inova Diagnostics, Inc. · Mar 2007
QUANTA LITE CELIAC DGP SCREEN
K062708 · Inova Diagnostics, Inc. · Dec 2006
QUANTA LITE GLIADIN IGG II
K052142 · Inova Diagnostics, Inc. · Oct 2005
QUANTA LITE GLIADIN IGA II
K052143 · Inova Diagnostics, Inc. · Oct 2005
DIAMEDIX IS-ANTI-GLIADIN IGG TEST SYSTEM
K012795 · Diamedix Corp. · Sep 2001