Cleared Traditional

K863794 - 3M IGG4 FAST TEST PACKAGE

K863794 is an FDA 510(k) clearance for 3M IGG4 FAST TEST PACKAGE, manufactured by 3M Company. The device is a Class 2 Immunology device with product code DHB cleared through the Traditional 510(k) pathway after a 68-day FDA review.

K863794 · 3M Company · Immunology device
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Dec 1986
Decision
68d
Days
Class 2
Risk

K863794 is an FDA 510(k) clearance for the 3M IGG4 FAST TEST PACKAGE. Classified as System, Test, Radioallergosorbent (rast) Immunological (product code DHB), Class II - Special Controls.

Submitted by 3M Company (Mountain View, US). The FDA issued a Cleared decision on December 3, 1986 after a review of 68 days - a notably fast clearance cycle.

This device falls under the Immunology FDA review panel, regulated under 21 CFR 866.5750 - 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 3M Company devices

FDA 510(k) Submission Details - K863794

510(k) Number K863794 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 26, 1986
Decision Date December 03, 1986
Days to Decision 68 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
37d faster than avg
Panel avg: 105d · This submission: 68d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DHB Device Classification - Class 2, Special Controls

Product Code DHB System, Test, Radioallergosorbent (rast) Immunological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.5750
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 - DHB System, Test, Radioallergosorbent (rast) Immunological

All 231
Devices cleared under the same product code (DHB) and FDA review panel - the closest regulatory comparables to K863794.
ALLERGEN SPECIFIC CONTROLS
K870152 · 3M Company · Feb 1987
SPECIFIC IGE FAST(TM) TEST II
K863967 · 3M Company · Dec 1986
BIOTECH'S IGE IMMUNO RESPONSE TEST ISOTOPE UNIT
K863743 · Immuno Nuclear Corp. · Dec 1986
ELM ALLERGEN DISC
K863973 · Immuno Nuclear Corp. · Dec 1986
IMMUNO BIOTECH'S LAMB'S QUARTERS ALLERGEN DISC
K863844 · Immuno Nuclear Corp. · Oct 1986
PHADEBAS RAST/PHADEZYM RAST ALLERTUBE
K863036 · Pharmacia, Inc. · Oct 1986