Cleared Traditional

K813392 - RADIOIMMUNOASSAY FOR HUMAN THYROID

K813392 is the FDA 510(k) clearance for RADIOIMMUNOASSAY FOR HUMAN THYROID by Leeco Diagnostics, Inc.. It is a Class 2 Chemistry device (product code JLW) cleared through the Traditional 510(k) pathway after a 19-day FDA review.

K813392 · Leeco Diagnostics, Inc. · Chemistry device
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Dec 1981
Decision
19d
Days
Class 2
Risk

K813392 is an FDA 510(k) clearance for the RADIOIMMUNOASSAY FOR HUMAN THYROID. Classified as Radioimmunoassay, Thyroid-stimulating Hormone (product code JLW), Class II - Special Controls.

Submitted by Leeco Diagnostics, Inc. (Mchenry, US). The FDA issued a Cleared decision on December 22, 1981 after a review of 19 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1690 - 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 Leeco Diagnostics, Inc. devices

Submission Details

510(k) Number K813392 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 03, 1981
Decision Date December 22, 1981
Days to Decision 19 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
69d faster than avg
Panel avg: 88d · This submission: 19d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JLW Radioimmunoassay, Thyroid-stimulating Hormone
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1690
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - JLW Radioimmunoassay, Thyroid-stimulating Hormone

All 145
Devices cleared under the same product code (JLW) and FDA review panel - the closest regulatory comparables to K813392.
QUANTIMUNE HTSH IRMA
K822291 · Bio-Rad · Aug 1982
MICROMEDIC HTSH RIA KIT
K813645 · Micromedic Systems · Jan 1982
IN VITRO DIAGNOSTIC RADIOIMMUNOASSAY
K813525 · Micromedic Systems · Dec 1981
AMERLEX TSH RIA KIT
K812136 · Amersham Corp. · Aug 1981
TECHNICON STAR SYSTEM
K811431 · Technicon Instruments Corp. · Jun 1981
TSH RADIOIMMUNOASSAY KIT
K802467 · American Diagnostic Corp. · Oct 1980