Cleared Traditional

K862447 - PANCOAT T3 UPTAKE COATED TUBE RADIOIMMU...

K862447 is the FDA 510(k) clearance for PANCOAT T3 UPTAKE COATED TUBE RADIOIMMU... by Pantex, Div. Bio-Analysis, Inc.. It is a Class 2 Chemistry device (product code KHQ) cleared through the Traditional 510(k) pathway after a 102-day FDA review.

K862447 · Pantex, Div. Bio-Analysis, Inc. · Chemistry device
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Oct 1986
Decision
102d
Days
Class 2
Risk

K862447 is an FDA 510(k) clearance for the PANCOAT T3 UPTAKE COATED TUBE RADIOIMMUNOASSAY KIT. Classified as Radioassay, Triiodothyronine Uptake (product code KHQ), Class II - Special Controls.

Submitted by Pantex, Div. Bio-Analysis, Inc. (Santa Monica, US). The FDA issued a Cleared decision on October 7, 1986 after a review of 102 days - within the typical 510(k) review window.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1715 - 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 Pantex, Div. Bio-Analysis, Inc. devices

Submission Details

510(k) Number K862447 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 27, 1986
Decision Date October 07, 1986
Days to Decision 102 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
14d slower than avg
Panel avg: 88d · This submission: 102d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KHQ Radioassay, Triiodothyronine Uptake
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1715
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 - KHQ Radioassay, Triiodothyronine Uptake

All 43
Devices cleared under the same product code (KHQ) and FDA review panel - the closest regulatory comparables to K862447.
CEDIA(TM) T UPTAKE
K872447 · Microgenics Corp. · Aug 1987
AFFINITY(TM) I UPTAKE IMMUNIT(TM)
K865083 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Jul 1987
CIBA CORNING MAGIC(R) LITE TU IMMUNOASSAY
K864132 · Ciba Corning Diagnostics Corp. · Dec 1986
STRAT THYROID UPTAKE FLUROMET ENZYME IMMUNOASSAY
K860422 · American Dade · Apr 1986
TERUMO SENSIBEAD EIA THYROID UPTAKE KIT
K842694 · Terumo Medical Corp. · Sep 1984
STRATUS THYROID UPTAKE FLUOROMETRIC
K834209 · American Dade · Mar 1984