Cleared Traditional

K992781 - ARCHITECH AFP MASTERCHECK

K992781 is the FDA 510(k) clearance for ARCHITECH AFP MASTERCHECK by Bio-Rad. It is a Class 1 Immunology device (product code JJX) cleared through the Traditional 510(k) pathway after a 230-day FDA review.

K992781 · Bio-Rad · Immunology device
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Apr 2000
Decision
230d
Days
Class 1
Risk

K992781 is an FDA 510(k) clearance for the ARCHITECH AFP MASTERCHECK, MODEL 6C01-05. Classified as Single (specified) Analyte Controls (assayed And Unassayed) (product code JJX), Class I - General Controls.

Submitted by Bio-Rad (Irvine, US). The FDA issued a Cleared decision on April 5, 2000 after a review of 230 days - an extended review cycle.

This device falls under the Immunology FDA review panel, regulated under 21 CFR 862.1660 - 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 Bio-Rad devices

Submission Details

510(k) Number K992781 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 19, 1999
Decision Date April 05, 2000
Days to Decision 230 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
126d slower than avg
Panel avg: 104d · This submission: 230d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JJX Single (specified) Analyte Controls (assayed And Unassayed)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1660
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 - JJX Single (specified) Analyte Controls (assayed And Unassayed)

All 371
Devices cleared under the same product code (JJX) and FDA review panel - the closest regulatory comparables to K992781.
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K000231 · Biosite Incorporated · Mar 2000
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K000230 · Biosite Incorporated · Feb 2000