Cleared Traditional

K851284 - RADIAL IMMUNO-DIFFUSION PLATES IGA, IGD, IGG & IGM

K851284 is an FDA 510(k) clearance for RADIAL IMMUNO-DIFFUSION PLATES IGA, manufactured by Cooper Biomedical, Inc.. The device is a Class 2 Immunology device with product code CZP cleared through the Traditional 510(k) pathway after a 71-day FDA review.

K851284 · Cooper Biomedical, Inc. · Immunology device
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Jun 1985
Decision
71d
Days
Class 2
Risk

K851284 is an FDA 510(k) clearance for the RADIAL IMMUNO-DIFFUSION PLATES IGA, IGD, IGG & IGM. Classified as Iga, Antigen, Antiserum, Control (product code CZP), Class II - Special Controls.

Submitted by Cooper Biomedical, Inc. (Malvern, US). The FDA issued a Cleared decision on June 11, 1985 after a review of 71 days - a notably fast clearance cycle.

This device falls under the Immunology FDA review panel, regulated under 21 CFR 866.5510 - 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 Cooper Biomedical, Inc. devices

FDA 510(k) Submission Details - K851284

510(k) Number K851284 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 01, 1985
Decision Date June 11, 1985
Days to Decision 71 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
34d faster than avg
Panel avg: 105d · This submission: 71d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CZP Device Classification - Class 2, Special Controls

Product Code CZP Iga, Antigen, Antiserum, Control
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.5510
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 - CZP Iga, Antigen, Antiserum, Control

All 48
Devices cleared under the same product code (CZP) and FDA review panel - the closest regulatory comparables to K851284.
DAKO ITA, IMMUNOGLOBULIN A (IGA)
K862183 · Dako Corp. · Aug 1986
IMMUNOGLOBULINS A,G,M,D,E IMMUNOLOGICAL TEST
K861167 · Atlantic Antibodies · Apr 1986
QUANTIMETRIC PLUS IGA REAGENT KIT
K855009 · Kallestad Laboratories, Inc. · Feb 1986
CORNING IMMUNOFIXATION SYS
K843614 · Corning Medical & Scientific · Oct 1984
TISSUE-TEK IMMUNOHISTOLOGY KIT IGA/IGG
K842468 · Miles Laboratories, Inc. · Aug 1984
AMER. HISTO-ID SYS PRIMARY IGA 2720-21
K842330 · Bartels Immunodiagnostic Supplies, Inc. · Aug 1984