Cleared Traditional

K830824 - URINE SCREENING KIT

K830824 is an FDA 510(k) clearance for URINE SCREENING KIT, manufactured by Syn-Kit, Inc.. The device is a Class 1 Microbiology device with product code CEN cleared through the Traditional 510(k) pathway after a 89-day FDA review.

K830824 · Syn-Kit, Inc. · Microbiology device
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Jun 1983
Decision
89d
Days
Class 1
Risk

K830824 is an FDA 510(k) clearance for the URINE SCREENING KIT. Classified as Dye-indicator, Ph (urinary, Non-quantitative) (product code CEN), Class I - General Controls.

Submitted by Syn-Kit, Inc. (Walker, US). The FDA issued a Cleared decision on June 12, 1983 after a review of 89 days - a notably fast clearance cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 862.1550 - the FDA microbiology device 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 Syn-Kit, Inc. devices

FDA 510(k) Submission Details - K830824

510(k) Number K830824 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 15, 1983
Decision Date June 12, 1983
Days to Decision 89 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
13d faster than avg
Panel avg: 102d · This submission: 89d
Pathway characteristics
Predicate-based equivalence.

CEN Device Classification - Class 1, General Controls

Product Code CEN Dye-indicator, Ph (urinary, Non-quantitative)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1550
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 - CEN Dye-indicator, Ph (urinary, Non-quantitative)

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