Cleared Traditional

K854944 - TDX IMMUNOGLOBULIN M DIAGNOSTIC KIT

K854944 is an FDA 510(k) clearance for TDX IMMUNOGLOBULIN M DIAGNOSTIC KIT, manufactured by Abbott Laboratories. The device is a Class 2 Immunology device with product code DAH cleared through the Traditional 510(k) pathway after a 260-day FDA review.

K854944 · Abbott Laboratories · Immunology device
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Aug 1986
Decision
260d
Days
Class 2
Risk

K854944 is an FDA 510(k) clearance for the TDX IMMUNOGLOBULIN M DIAGNOSTIC KIT. Classified as Gamma Globulin, Antigen, Antiserum, Control (product code DAH), Class II - Special Controls.

Submitted by Abbott Laboratories (Irving, US). The FDA issued a Cleared decision on August 27, 1986 after a review of 260 days - an extended review 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: 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.

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FDA 510(k) Submission Details - K854944

510(k) Number K854944 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 10, 1985
Decision Date August 27, 1986
Days to Decision 260 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
156d slower than avg
Panel avg: 104d · This submission: 260d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DAH Device Classification - Class 2, Special Controls

Product Code DAH Gamma Globulin, 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.