Cleared Traditional

K943436 - URINE REAGENT STRIPS-8 PARAMETERS

K943436 is an FDA 510(k) clearance for URINE REAGENT STRIPS-8 PARAMETERS, manufactured by Teco Diagnostics. The device is a Class 1 Chemistry device with product code JJB cleared through the Traditional 510(k) pathway after a 280-day FDA review.

K943436 · Teco Diagnostics · Chemistry device
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Apr 1995
Decision
280d
Days
Class 1
Risk

K943436 is an FDA 510(k) clearance for the URINE REAGENT STRIPS-8 PARAMETERS. Classified as Azo-dyes, Colorimetric, Bilirubin & Its Conjugates (urinary, Non-quant.) (product code JJB), Class I - General Controls.

Submitted by Teco Diagnostics (Placentia, US). The FDA issued a Cleared decision on April 24, 1995 after a review of 280 days - an extended review cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1115 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Chemistry review framework, consistent with the majority of Class II 510(k) submissions.

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FDA 510(k) Submission Details - K943436

510(k) Number K943436 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 18, 1994
Decision Date April 24, 1995
Days to Decision 280 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
192d slower than avg
Panel avg: 88d · This submission: 280d
Pathway characteristics
Predicate-based equivalence.

JJB Device Classification - Class 1, General Controls

Product Code JJB Azo-dyes, Colorimetric, Bilirubin & Its Conjugates (urinary, Non-quant.)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1115
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.