Cleared Traditional

K031873 - I-STAT CARDIAC MARKERS CONTROL LEVEL 1, 2, AND 3 (FDA 510(k) Clearance)

Also includes:
CARDIAC MARKERS CALIBRATION VERIFICATION CONTROL SET

Class I Chemistry device.

K031873 · I-Stat Corporation · Chemistry device
Download Printable Device Report (PDF)
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Oct 2003
Decision
112d
Days
Class 1
Risk

K031873 is an FDA 510(k) clearance for the I-STAT CARDIAC MARKERS CONTROL LEVEL 1, 2, AND 3. Classified as Single (specified) Analyte Controls (assayed And Unassayed) (product code JJX), Class I - General Controls.

Submitted by I-Stat Corporation (East Windsor, US). The FDA issued a Cleared decision on October 7, 2003 after a review of 112 days - within the typical 510(k) review window.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1660 - 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.

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Submission Details

510(k) Number K031873 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 17, 2003
Decision Date October 07, 2003
Days to Decision 112 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
24d slower than avg
Panel avg: 88d · This submission: 112d
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.