Cleared Traditional

K982533 - UNICAP GLIADIN IGA ASSAY

K982533 is an FDA 510(k) clearance for UNICAP GLIADIN IGA ASSAY, manufactured by Pharmacia & Upjohn Co.. The device is a Class 2 Immunology device with product code MST cleared through the Traditional 510(k) pathway after a 94-day FDA review.

K982533 · Pharmacia & Upjohn Co. · Immunology device
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Oct 1998
Decision
94d
Days
Class 2
Risk

K982533 is an FDA 510(k) clearance for the UNICAP GLIADIN IGA ASSAY. Classified as Antibodies, Gliadin (product code MST), Class II - Special Controls.

Submitted by Pharmacia & Upjohn Co. (Kalamazoo, US). The FDA issued a Cleared decision on October 22, 1998 after a review of 94 days - within the typical 510(k) review window.

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 Pharmacia & Upjohn Co. devices

FDA 510(k) Submission Details - K982533

510(k) Number K982533 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 20, 1998
Decision Date October 22, 1998
Days to Decision 94 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
11d faster than avg
Panel avg: 105d · This submission: 94d
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 28
Devices cleared under the same product code (MST) and FDA review panel - the closest regulatory comparables to K982533.
THE APTUS (AUTOMATED) APPLICATION OF THE GLIADIN IGG ELISA TEST SYSTEM.
K993250 · Zeus Scientific, Inc. · Nov 1999
GLIADIN IGG ELISA TEST SYSTEM
K990204 · Zeus Scientific, Inc. · Mar 1999
GLIADIN IGA ELISA TEST SYSTEM
K990207 · Zeus Scientific, Inc. · Mar 1999
UNICAP GLIADIN IGG ASSAY
K982701 · Pharmacia & Upjohn Co. · Oct 1998
BINDAZYME ANTIGLIADIN IGG
K981644 · The Binding Site, Ltd. · Sep 1998
BINDAZYME ANTIGLIADIN IGG/IGA COMBI KIT
K981929 · The Binding Site, Ltd. · Sep 1998