Cleared Traditional

K914467 - MILENIA TOTAL T3

K914467 is the FDA 510(k) clearance for MILENIA TOTAL T3 by Diagnostic Products Corp.. It is a Class 2 Chemistry device (product code CDP) cleared through the Traditional 510(k) pathway after a 122-day FDA review.

K914467 · Diagnostic Products Corp. · Chemistry device
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Feb 1992
Decision
122d
Days
Class 2
Risk

K914467 is an FDA 510(k) clearance for the MILENIA TOTAL T3. Classified as Radioimmunoassay, Total Triiodothyronine (product code CDP), Class II - Special Controls.

Submitted by Diagnostic Products Corp. (Los Angeles, US). The FDA issued a Cleared decision on February 6, 1992 after a review of 122 days - within the typical 510(k) review window.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1710 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Chemistry review framework, consistent with the majority of Class II 510(k) submissions.

View all Diagnostic Products Corp. devices

Submission Details

510(k) Number K914467 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 07, 1991
Decision Date February 06, 1992
Days to Decision 122 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
34d slower than avg
Panel avg: 88d · This submission: 122d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code CDP Radioimmunoassay, Total Triiodothyronine
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1710
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 - CDP Radioimmunoassay, Total Triiodothyronine

All 78
Devices cleared under the same product code (CDP) and FDA review panel - the closest regulatory comparables to K914467.
KODAK AMERLEX MAB FT3 ASSAY
K922771 · Eastman Kodak Company · Oct 1992
TECHNICON IMMUNO 1 SYSTEM TOTAL TRIIODOTHYRONINE
K923258 · Heraeus Kulzer, Inc. · Sep 1992
TOTAL T3 CHEMILUMINESCENCE ASSAY
K923015 · Nichols Institute Diagnostics · Sep 1992
IMX FREE TRIIODOTHYRONINE
K905261 · Abbott Laboratories · Jan 1991
TDX FREE T3 CALCULATION
K903433 · Abbott Laboratories · Oct 1990
CEDIA TOTAL T3 ASSAY
K904098 · Microgenics Corp. · Sep 1990