Cleared Traditional

K832154 - DHEA-SULFATE I RIA KIT

K832154 is the FDA 510(k) clearance for DHEA-SULFATE I RIA KIT by Diagnostic Systems Laboratories, Inc.. It is a Class 1 Chemistry device (product code JKC) cleared through the Traditional 510(k) pathway after a 42-day FDA review.

K832154 · Diagnostic Systems Laboratories, Inc. · Chemistry device
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Aug 1983
Decision
42d
Days
Class 1
Risk

K832154 is an FDA 510(k) clearance for the DHEA-SULFATE I RIA KIT. Classified as Radioimmunoassay, Dehydroepiandrosterone (free And Sulfate) (product code JKC), Class I - General Controls.

Submitted by Diagnostic Systems Laboratories, Inc. (Walker, US). The FDA issued a Cleared decision on August 16, 1983 after a review of 42 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1245 - 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 Diagnostic Systems Laboratories, Inc. devices

Submission Details

510(k) Number K832154 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 05, 1983
Decision Date August 16, 1983
Days to Decision 42 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
46d faster than avg
Panel avg: 88d · This submission: 42d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JKC Radioimmunoassay, Dehydroepiandrosterone (free And Sulfate)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1245
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 - JKC Radioimmunoassay, Dehydroepiandrosterone (free And Sulfate)

All 14
Devices cleared under the same product code (JKC) and FDA review panel - the closest regulatory comparables to K832154.
ACTIVE DHEA-SULFATE DSL3500
K851239 · Diagnostic Systems Laboratories, Inc. · Apr 1985
COAT-A-COUNT DHEA-SO4 RIA KIT
K842552 · Diagnostic Products Corp. · Aug 1984
COAT-A-COUNT DHEA RIA KIT
K842606 · Diagnostic Products Corp. · Aug 1984
DHEA-SULFATE DIRECT RIA KIT(125I)
K811906 · Immunalysis Corporation · Jul 1981