Cleared Abbreviated

K132391 - IMMULITE 2000 ANTI-TG AB CALIBRATION VERIFICATION MATERIAL, IMMULITE 2000 ANTI-TPO AB CALIBRATION VERIFICATIN MATERIAL

K132391 is an FDA 510(k) clearance for IMMULITE 2000 ANTI-TG AB CALIBRATION VE..., manufactured by Siemens Helathcare Diagnostics, Inc.. The device is a Class 1 Immunology device with product code JJX cleared through the Abbreviated 510(k) pathway after a 50-day FDA review.

K132391 · Siemens Helathcare Diagnostics, Inc. · Immunology device
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Optimized for regulatory review, auditing and printing
Sep 2013
Decision
50d
Days
Class 1
Risk

K132391 is an FDA 510(k) clearance for the IMMULITE 2000 ANTI-TG AB CALIBRATION VERIFICATION MATERIAL, IMMULITE 2000 ANT.... Classified as Single (specified) Analyte Controls (assayed And Unassayed) (product code JJX), Class I - General Controls.

Submitted by Siemens Helathcare Diagnostics, Inc. (Tarrytown, US). The FDA issued a Cleared decision on September 20, 2013 after a review of 50 days - a notably fast clearance cycle.

This device falls under the Immunology FDA review panel, regulated under 21 CFR 862.1660 - the FDA immunology device framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Siemens Helathcare Diagnostics, Inc. devices

FDA 510(k) Submission Details - K132391

510(k) Number K132391 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 01, 2013
Decision Date September 20, 2013
Days to Decision 50 days
Submission Type Abbreviated
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
55d faster than avg
Panel avg: 105d · This submission: 50d
Pathway characteristics
Standards-based clearance path.

JJX Device Classification - Class 1, General Controls

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 445
Devices cleared under the same product code (JJX) and FDA review panel - the closest regulatory comparables to K132391.
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