Cleared Traditional

K860251 - AMERLEX-M T4 RIA KIT FOR SERUM AND PLASMA

K860251 is an FDA 510(k) clearance for AMERLEX-M T4 RIA KIT FOR SERUM AND PLASMA, manufactured by Amersham Corp.. The device is a Class 2 Chemistry device with product code CEC cleared through the Traditional 510(k) pathway after a 18-day FDA review.

K860251 · Amersham Corp. · Chemistry device
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Feb 1986
Decision
18d
Days
Class 2
Risk

K860251 is an FDA 510(k) clearance for the AMERLEX-M T4 RIA KIT FOR SERUM AND PLASMA. Classified as Radioimmunoassay, Free Thyroxine (product code CEC), Class II - Special Controls.

Submitted by Amersham Corp. (Arlington Heights, US). The FDA issued a Cleared decision on February 11, 1986 after a review of 18 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1695 - 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 Amersham Corp. devices

FDA 510(k) Submission Details - K860251

510(k) Number K860251 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 24, 1986
Decision Date February 11, 1986
Days to Decision 18 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
70d faster than avg
Panel avg: 88d · This submission: 18d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CEC Device Classification - Class 2, Special Controls

Product Code CEC Radioimmunoassay, Free Thyroxine
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1695
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 - CEC Radioimmunoassay, Free Thyroxine

All 66
Devices cleared under the same product code (CEC) and FDA review panel - the closest regulatory comparables to K860251.
IQ FTI IMMUNOASSAY
K865104 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Mar 1987
IQ FREE T4 IMMUNOASSAY
K864658 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Mar 1987
SIMULTRAC FREE T4[57CO]/TSH MAB[125I]
K864838 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Feb 1987
SIMULTRAC FREE T4(57CO)/TSH[125I] RADIOIMMUNOASSAY
K853628 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Sep 1985
AMERLEX-M FREE T-4 RADIOIMMUNOASSAY KIT
K842482 · Amersham Corp. · Aug 1984
CORNING MAGIC SINGLE STEP FREE T4
K832381 · Corning Medical & Scientific · Sep 1983