Cleared Traditional

GLUCOSE 3, INLAB REAGENT STRIPS-URINALY (K831499) - FDA 510(k) Clearance

Class I Chemistry device.

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Jun 1983
Decision
37d
Days
Class 1
Risk

K831499 is an FDA 510(k) clearance for the GLUCOSE 3, INLAB REAGENT STRIPS-URINALY. Classified as Nitroprusside, Ketones (urinary, Non-quant.) (product code JIN), Class I - General Controls.

Submitted by Laprol Scientific, Inc. (Mchenry, US). The FDA issued a Cleared decision on June 17, 1983 after a review of 37 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1435 - 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 Laprol Scientific, Inc. devices

Submission Details

510(k) Number K831499 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 11, 1983
Decision Date June 17, 1983
Days to Decision 37 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
51d faster than avg
Panel avg: 88d · This submission: 37d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JIN Nitroprusside, Ketones (urinary, Non-quant.)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1435
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 - JIN Nitroprusside, Ketones (urinary, Non-quant.)

All 10
Devices cleared under the same product code (JIN) and FDA review panel - the closest regulatory comparables to K831499.
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SIGMS B-HYDROXYBUTARATE PROCEDURE NO. 310-UV
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HELENA BIOSTRIP K
K830976 · Helena Laboratories · May 1983
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K801270 · Miles Laboratories, Inc. · Jul 1980