Cleared Traditional

K854756 - SHORT RAGWEED ALLERGEN DISC

K854756 is the FDA 510(k) clearance for SHORT RAGWEED ALLERGEN DISC by Immuno Nuclear Corp.. It is a Class 2 Immunology device (product code DHB) cleared through the Traditional 510(k) pathway after a 169-day FDA review.

K854756 · Immuno Nuclear Corp. · Immunology device
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May 1986
Decision
169d
Days
Class 2
Risk

K854756 is an FDA 510(k) clearance for the SHORT RAGWEED ALLERGEN DISC. Classified as System, Test, Radioallergosorbent (rast) Immunological (product code DHB), Class II - Special Controls.

Submitted by Immuno Nuclear Corp. (Stillwater, US). The FDA issued a Cleared decision on May 15, 1986 after a review of 169 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Immunology review framework, consistent with the majority of Class II 510(k) submissions.

View all Immuno Nuclear Corp. devices

Submission Details

510(k) Number K854756 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 27, 1985
Decision Date May 15, 1986
Days to Decision 169 days
Submission Type Traditional
Review Panel Immunology (IM)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
65d slower than avg
Panel avg: 104d · This submission: 169d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 200
Devices cleared under the same product code (DHB) and FDA review panel - the closest regulatory comparables to K854756.
PHADEBAS RAST/PHADEZYM RAST ALLERTUBE
K863036 · Pharmacia, Inc. · Oct 1986
PHADIOTOP (TM) RIA/PHADIOTOP (TM) EIA
K863355 · Pharmacia, Inc. · Sep 1986
VENTRESCREEN II POLLENS ENZYME IMMUNOASSAY
K862901 · Ventrex Laboratories, Inc. · Sep 1986
PHADEBAS RAST/PHADEZYM RAST TEST ALLERGEN DISCS
K861184 · Pharmacia, Inc. · Apr 1986
PHADEBAS RAST PHADEZYM RAST DISCS FX2,FX3 & FX5
K854865 · Pharmacia, Inc. · Apr 1986
PHADEBAS RAST/PHADEZYM RAST ALLERTUBES
K854939 · Pharmacia, Inc. · Feb 1986