Cleared Traditional

K771135 - QUANTIMUNE NEONATAL & THYROXINE RIA

K771135 is an FDA 510(k) clearance for QUANTIMUNE NEONATAL & THYROXINE RIA, manufactured by Bio-Rad. The device is a Class 2 Immunology device with product code CDX cleared through the Traditional 510(k) pathway after a 21-day FDA review.

K771135 · Bio-Rad · Immunology device
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Jul 1977
Decision
21d
Days
Class 2
Risk

K771135 is an FDA 510(k) clearance for the QUANTIMUNE NEONATAL & THYROXINE RIA. Classified as Radioimmunoassay, Total Thyroxine (product code CDX), Class II - Special Controls.

Submitted by Bio-Rad (Mchenry, US). The FDA issued a Cleared decision on July 14, 1977 after a review of 21 days - a notably fast clearance cycle.

This device falls under the Immunology FDA review panel, regulated under 21 CFR 862.1700 - the FDA immunology device 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 Bio-Rad devices

FDA 510(k) Submission Details - K771135

510(k) Number K771135 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 23, 1977
Decision Date July 14, 1977
Days to Decision 21 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
84d faster than avg
Panel avg: 105d · This submission: 21d
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 Immunology 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 K771135.
AMES T-4 STRIP TEST
K772014 · Miles Laboratories, Inc. · Nov 1977
T4 RIA TEST SYSTEM
K771221 · Monobind · Aug 1977
RIA FOR TOTAL THYROXINE
K771309 · Abbott Laboratories · Aug 1977
REAGENT SYSTEM, THYROXINE, ARIA
K770733 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Jun 1977
REAGENT SET, T-4, CPB
K770737 · G.D. Searle and Co. · Jun 1977
TOTAL THYROXINE (RIA) REAGENT SET
K770940 · The Dow Chemical Co. · Jun 1977