Cleared Traditional

CARDIOCHEX CKMB IMMUNOINHIBITION CONTROL (K944247) - FDA 510(k) Clearance

Class I Chemistry device.

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Oct 1994
Decision
61d
Days
Class 1
Risk

K944247 is an FDA 510(k) clearance for the CARDIOCHEX CKMB IMMUNOINHIBITION CONTROL. Classified as Enzyme Controls (assayed And Unassayed) (product code JJT), Class I - General Controls.

Submitted by Cala Diagnostics (Grover Beach, US). The FDA issued a Cleared decision on October 31, 1994 after a review of 61 days - a notably fast clearance cycle.

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: 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 Cala Diagnostics devices

Submission Details

510(k) Number K944247 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 31, 1994
Decision Date October 31, 1994
Days to Decision 61 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
27d faster than avg
Panel avg: 88d · This submission: 61d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JJT Enzyme 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 - JJT Enzyme Controls (assayed And Unassayed)

All 96
Devices cleared under the same product code (JJT) and FDA review panel - the closest regulatory comparables to K944247.
LIQUICHEK CARDIAC MARKERS CONTROL LT LEVEL 1, 2, 3, AND TRILEVEL
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K980556 · Bio-Rad · Feb 1998
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LIQUICHEK CARDIAC MARKERS CONTROL (CAT. NO. 685,686,687,688)
K961828 · Bio-Rad · Jun 1996