Cleared Traditional

K874802 - FLIPSCREEN QAT

K874802 is the FDA 510(k) clearance for FLIPSCREEN QAT by Alerchek, Inc.. It is a Class 2 Immunology device (product code DHB) cleared through the Traditional 510(k) pathway after a 86-day FDA review.

K874802 · Alerchek, Inc. · Immunology device
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Feb 1988
Decision
86d
Days
Class 2
Risk

K874802 is an FDA 510(k) clearance for the FLIPSCREEN QAT. Classified as System, Test, Radioallergosorbent (rast) Immunological (product code DHB), Class II - Special Controls.

Submitted by Alerchek, Inc. (Portland, US). The FDA issued a Cleared decision on February 17, 1988 after a review of 86 days - a notably fast clearance 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: 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 Alerchek, Inc. devices

Submission Details

510(k) Number K874802 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 23, 1987
Decision Date February 17, 1988
Days to Decision 86 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
18d faster than avg
Panel avg: 104d · This submission: 86d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DHB System, Test, Radioallergosorbent (rast) Immunological
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 - DHB System, Test, Radioallergosorbent (rast) Immunological

All 200
Devices cleared under the same product code (DHB) and FDA review panel - the closest regulatory comparables to K874802.
QUIDEL TOTAL IGE TEST
K875168 · Quidel Corp. · Mar 1988
ADDITIONAL ALLERGENS FOR IGE FAST-PLUS TEST
K880003 · Em Diagnostic Systems, Inc. · Mar 1988
MULTI-ALLERGEN IGE FAST SCREEN III D1,E1,G6,M2,T3
K880001 · 3M Company · Feb 1988
TOTAL IGE IMMUNO RESPONSE TEST (IRT(R))
K875274 · Incstar Corp. · Feb 1988
MULTI-ALLERGEN IGE FAST SCREEN (MOLDS)
K880002 · 3M Company · Feb 1988
MULTI-ALLERGEN IGE FAST SCREEN (ENVIRONMENTAL)
K874446 · 3M Company · Dec 1987