Cleared Traditional

K862174 - TIMOTHY ALLERGEN DISC

K862174 is the FDA 510(k) clearance for TIMOTHY ALLERGEN DISC by Immuno Nuclear Corp.. It is a Class 2 Immunology device (product code DGC) cleared through the Traditional 510(k) pathway after a 58-day FDA review.

K862174 · Immuno Nuclear Corp. · Immunology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 1986
Decision
58d
Days
Class 2
Risk

K862174 is an FDA 510(k) clearance for the TIMOTHY ALLERGEN DISC. Classified as Ige, Antigen, Antiserum, Control (product code DGC), Class II - Special Controls.

Submitted by Immuno Nuclear Corp. (Stillwater, US). The FDA issued a Cleared decision on August 6, 1986 after a review of 58 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 Immuno Nuclear Corp. devices

Submission Details

510(k) Number K862174 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 09, 1986
Decision Date August 06, 1986
Days to Decision 58 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
46d faster than avg
Panel avg: 104d · This submission: 58d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DGC Ige, 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 - DGC Ige, Antigen, Antiserum, Control

All 84
Devices cleared under the same product code (DGC) and FDA review panel - the closest regulatory comparables to K862174.
ALLEIA TOTAL IGE IRMA W/MONO. ANTI. RKIE 1,2,5
K872913 · Diagnostic Products Corp. · Sep 1987
TANDEM-M IMMUNOENZYMETRIC ASSAY FOR IGE--
K863858 · Hybritech, Inc. · Nov 1986
ENZYMUN-TEST(R) IGE
K863822 · Boehringer Mannheim Corp. · Oct 1986
QUIDEL ALLERGY SCREEN
K861171 · Quidel Corp. · Apr 1986
TOTAL IGE-IRMA RIA KIT
K860032 · Diagnostic Products Corp. · Apr 1986
EIA MONOCLONAL TOTAL IGE KIT
K860033 · Diagnostic Products Corp. · Apr 1986