Cleared Traditional

MULTISTAT III TRIGLYCERIDE TEST (K771472) - FDA 510(k) Clearance

Class I Chemistry device.

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Sep 1977
Decision
29d
Days
Class 1
Risk

K771472 is an FDA 510(k) clearance for the MULTISTAT III TRIGLYCERIDE TEST. Classified as Lipase Hydrolysis/glycerol Kinase Enzyme, Triglycerides (product code CDT), Class I - General Controls.

Submitted by Instrumentation Laboratory CO (Mchenry, US). The FDA issued a Cleared decision on September 2, 1977 after a review of 29 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1705 - 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 Instrumentation Laboratory CO devices

Submission Details

510(k) Number K771472 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 04, 1977
Decision Date September 02, 1977
Days to Decision 29 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
59d faster than avg
Panel avg: 88d · This submission: 29d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code CDT Lipase Hydrolysis/glycerol Kinase Enzyme, Triglycerides
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1705
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 - CDT Lipase Hydrolysis/glycerol Kinase Enzyme, Triglycerides

All 150
Devices cleared under the same product code (CDT) and FDA review panel - the closest regulatory comparables to K771472.
A-GENT TRIGLLYCERIDES GPO
K874187 · Abbott Laboratories · Jan 1988
IQ TRIGLYCERIDES
K864268 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Dec 1986
VISION TRIGLYCERIDES
K850031 · Abbott Laboratories · Feb 1985
QCA TRIGLYCERIDES
K842891 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Aug 1984
DELTA TEST TRIGLYCERIDES
K802136 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Oct 1980
A-GENT TRIGLYCERIDES
K771608 · Abbott Laboratories · Sep 1977