Cleared Traditional

K831107 - COAT-A-COUNT NEONATAL T4 KIT RIA KIT

K831107 is an FDA 510(k) clearance for COAT-A-COUNT NEONATAL T4 KIT RIA KIT, manufactured by Diagnostic Products Corp.. The device is a Class 2 Chemistry device with product code CDX cleared through the Traditional 510(k) pathway after a 43-day FDA review.

K831107 · Diagnostic Products Corp. · Chemistry device
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May 1983
Decision
43d
Days
Class 2
Risk

K831107 is an FDA 510(k) clearance for the COAT-A-COUNT NEONATAL T4 KIT RIA KIT. Classified as Radioimmunoassay, Total Thyroxine (product code CDX), Class II - Special Controls.

Submitted by Diagnostic Products Corp. (Mchenry, US). The FDA issued a Cleared decision on May 18, 1983 after a review of 43 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1700 - 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 Diagnostic Products Corp. devices

FDA 510(k) Submission Details - K831107

510(k) Number K831107 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 05, 1983
Decision Date May 18, 1983
Days to Decision 43 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
45d faster than avg
Panel avg: 88d · This submission: 43d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CDX Device Classification - Class 2, Special Controls

Product Code CDX Radioimmunoassay, Total Thyroxine
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1700
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 - CDX Radioimmunoassay, Total Thyroxine

All 93
Devices cleared under the same product code (CDX) and FDA review panel - the closest regulatory comparables to K831107.
STRAT TOTAL THYROXINE FLUOROMET ENZYME IMMUNOASSAY
K860421 · American Dade · Feb 1986
T4 RIA
K833850 · Syncor Intl. Corp. · Jan 1984
MAGIC T4 125I RADIOIMMUNOASSAY
K831533 · Corning Medical & Scientific · Jun 1983
MONOCLONAL ANTIBODY T4 RADIO-KIT
K823265 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Dec 1982
NML-TETRA-TUBE RIA
K823053 · Nuclear Medical Laboratories, Inc. · Nov 1982
LEECO T4 QUANT DIAGNOSTICS TEST KIT
K822399 · Leeco Diagnostics, Inc. · Sep 1982