Cleared Traditional

K830288 - TRIGLYCERIDE DIAGNOSTIC KIT

K830288 is the FDA 510(k) clearance for TRIGLYCERIDE DIAGNOSTIC KIT by Sclavo, Inc.. It is a Class 1 Chemistry device (product code CDT) cleared through the Traditional 510(k) pathway after a 29-day FDA review.

K830288 · Sclavo, Inc. · Chemistry device
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Feb 1983
Decision
29d
Days
Class 1
Risk

K830288 is an FDA 510(k) clearance for the TRIGLYCERIDE DIAGNOSTIC KIT. Classified as Lipase Hydrolysis/glycerol Kinase Enzyme, Triglycerides (product code CDT), Class I - General Controls.

Submitted by Sclavo, Inc. (Mchenry, US). The FDA issued a Cleared decision on February 25, 1983 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 Sclavo, Inc. devices

Submission Details

510(k) Number K830288 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 27, 1983
Decision Date February 25, 1983
Days to Decision 29 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
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 112
Devices cleared under the same product code (CDT) and FDA review panel - the closest regulatory comparables to K830288.
SERALYZER TRIGLYCERIDES REAGENT STRIPS
K832684 · Miles Laboratories, Inc. · Oct 1983
ENZYMATIC TRIGLYCERIDES #2000
K832444 · Stanbio Laboratory · Aug 1983
TRIGLYCERIDES REAGENT SET
K831858 · Stanbio Laboratory · Jul 1983
TRIGLYCERIDE REAGENT (UV)
K823709 · Gilford Diagnostics · Jan 1983
ULTRA CHEM E-TRIG #65024
K812589 · Harleco · Sep 1981
SPIN-CHEM TRIGLYCERIDES REAGENT
K812471 · Smithkline Diagnostics, Inc. · Sep 1981