Cleared Traditional

LIPOPHOR(TM) SYST, HUMAN SERUM LIPOPROTEIN CONTROL (K883247) - FDA 510(k) Clearance

Class I Chemistry device.

K883247 · Quantimetrix Medical Industries · Chemistry device
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Sep 1988
Decision
42d
Days
Class 1
Risk

K883247 is an FDA 510(k) clearance for the LIPOPHOR(TM) SYST, HUMAN SERUM LIPOPROTEIN CONTROL. Classified as Multi-analyte Controls, All Kinds (assayed) (product code JJY), Class I - General Controls.

Submitted by Quantimetrix Medical Industries (Hawthorne, US). The FDA issued a Cleared decision on September 13, 1988 after a review of 42 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 Quantimetrix Medical Industries devices

Submission Details

510(k) Number K883247 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 02, 1988
Decision Date September 13, 1988
Days to Decision 42 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
46d faster than avg
Panel avg: 88d · This submission: 42d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JJY Multi-analyte Controls, All Kinds (assayed)
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 - JJY Multi-analyte Controls, All Kinds (assayed)

All 166
Devices cleared under the same product code (JJY) and FDA review panel - the closest regulatory comparables to K883247.
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K881503 · Baxter Healthcare Corp · Jul 1988
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