Cleared Traditional

K924594 - DELFIA DIGOXIN KIT

K924594 is the FDA 510(k) clearance for DELFIA DIGOXIN KIT by Wallac OY. It is a Class 2 Toxicology device (product code KXT) cleared through the Traditional 510(k) pathway after a 98-day FDA review.

K924594 · Wallac OY · Toxicology device
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Dec 1992
Decision
98d
Days
Class 2
Risk

K924594 is an FDA 510(k) clearance for the DELFIA DIGOXIN KIT. Classified as Enzyme Immunoassay, Digoxin (product code KXT), Class II - Special Controls.

Submitted by Wallac OY (Finland, FI). The FDA issued a Cleared decision on December 17, 1992 after a review of 98 days - within the typical 510(k) review window.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.3320 - the FDA toxicology 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 Toxicology review framework, consistent with the majority of Class II 510(k) submissions.

View all Wallac OY devices

Submission Details

510(k) Number K924594 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 10, 1992
Decision Date December 17, 1992
Days to Decision 98 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
11d slower than avg
Panel avg: 87d · This submission: 98d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KXT Enzyme Immunoassay, Digoxin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.3320
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 Toxicology devices follow this clearance model.

Regulatory Peers - KXT Enzyme Immunoassay, Digoxin

All 70
Devices cleared under the same product code (KXT) and FDA review panel - the closest regulatory comparables to K924594.
ACS DIGOXIN IMMUNOASSAY
K931213 · Ciba Corning Diagnostics Corp. · Jun 1993
ACA DIGOXIN ANALYTICAL TEST PACK
K930162 · E.I. Dupont DE Nemours & Co., Inc. · Mar 1993
ACCESS DIGOXIN ASSAY
K925802 · Bio-Rad Laboratories, Inc. · Jan 1993
CEDIA DIGOXIN PLUS ASSAY
K923853 · Microgenics Corp. · Sep 1992
CEDIA DIGOXIN ASSAY (MODIFICATION)
K920214 · Microgenics Corp. · Mar 1992
IL TEST(TM DIGOXIN
K914151 · Instrumentation Laboratory CO · Nov 1991