Cleared Traditional

K810381 - HTSH RIABEAD DIAGNOSTIC KIT

K810381 is an FDA 510(k) clearance for HTSH RIABEAD DIAGNOSTIC KIT, manufactured by Abbott Laboratories. The device is a Class 1 Chemistry device with product code CGJ cleared through the Traditional 510(k) pathway after a 13-day FDA review.

K810381 · Abbott Laboratories · Chemistry device
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Feb 1981
Decision
13d
Days
Class 1
Risk

K810381 is an FDA 510(k) clearance for the HTSH RIABEAD DIAGNOSTIC KIT. Classified as Radioimmunoassay, Follicle-stimulating Hormone (product code CGJ), Class I - General Controls.

Submitted by Abbott Laboratories (Abbott Park, US). The FDA issued a Cleared decision on February 26, 1981 after a review of 13 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1300 - 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 Abbott Laboratories devices

FDA 510(k) Submission Details - K810381

510(k) Number K810381 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 13, 1981
Decision Date February 26, 1981
Days to Decision 13 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
75d faster than avg
Panel avg: 88d · This submission: 13d
Pathway characteristics
Predicate-based equivalence.

CGJ Device Classification - Class 1, General Controls

Product Code CGJ Radioimmunoassay, Follicle-stimulating Hormone
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1300
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 - CGJ Radioimmunoassay, Follicle-stimulating Hormone

All 58
Devices cleared under the same product code (CGJ) and FDA review panel - the closest regulatory comparables to K810381.
FOLLICLE STIMULATING HORMONE DIRECT RIA
K811905 · Immunalysis Corporation · Jul 1981
FOLLICLE STIMULATING HORMONE ANTISERUM
K810852 · Pcl-Ria, Inc. · Apr 1981
LEECO FSH-QUANT DIAGNOSTIC KIT
K810663 · Leeco Diagnostics, Inc. · Mar 1981
FOLLICE STIMULATING HORMONE-RADIOIMM. KT
K803279 · Immuno Nuclear Corp. · Jan 1981
CENTRIA FSH RIA
K792233 · Union Carbide Corp. · Jan 1980
QUANTIMUNE HFSH RIA
K791836 · Bio-Rad · Oct 1979