Cleared Traditional

K073612 - URIC ACID (AOX), SCAL, NORTROL, ABTROL

K073612 is an FDA 510(k) clearance for URIC ACID (AOX), manufactured by Thermofisher Scientific OY. The device is a Class 2 Chemistry device with product code JIX cleared through the Traditional 510(k) pathway after a 154-day FDA review.

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May 2008
Decision
154d
Days
Class 2
Risk

K073612 is an FDA 510(k) clearance for the URIC ACID (AOX), SCAL, NORTROL, ABTROL. Classified as Calibrator, Multi-analyte Mixture (product code JIX), Class II - Special Controls.

Submitted by Thermofisher Scientific OY (Vantaa, FI). The FDA issued a Cleared decision on May 23, 2008 after a review of 154 days - an extended review cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1150 - the FDA in vitro diagnostics and chemistry 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 Chemistry review framework, consistent with the majority of Class II 510(k) submissions.

View all Thermofisher Scientific OY devices

FDA 510(k) Submission Details - K073612

510(k) Number K073612 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 21, 2007
Decision Date May 23, 2008
Days to Decision 154 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
66d slower than avg
Panel avg: 88d · This submission: 154d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JIX Device Classification - Class 2, Special Controls

Product Code JIX Calibrator, Multi-analyte Mixture
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1150
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 Chemistry devices follow this clearance model.

Regulatory Peers - JIX Calibrator, Multi-analyte Mixture

All 262
Devices cleared under the same product code (JIX) and FDA review panel - the closest regulatory comparables to K073612.
STA - FREE PS CALIBRATOR
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K081103 · Siemens Healthcare Diagnostics, Inc. · May 2008
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K080607 · Roche Diagnostics Corp. · May 2008
ABX PENTRA URINE CAL
K071779 · Horiba Abx · Mar 2008