Amerlite Digoxin Assay, LAN.0700/2700, 240/144 Kit

FDA 510(k) K880823 · Amersham Corp.

Substantially Equivalent

510(k) numberK880823

Submission

Device name
Amerlite Digoxin Assay, LAN.0700/2700, 240/144 Kit
Applicant
Amersham Corp.
Arlington Heights, IL, US
Received
March 1, 1988
Decision date
May 31, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KXT – Enzyme Immunoassay, Digoxin
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3320
Specialty
Clinical Toxicology

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K082953Architect Idigoxin and Architect Idigoxin Calibrators, Models 1P32-25 and IP32-01KXT · Traditional Biokit, S.A.12/22/2008SE
K061249Axsym Digoxin IIIKXT · Special Abbott Laboratories06/02/2006SE
K033007Bayer Advia Digoxin Assay for the Integrated Module SystemKXT · Traditional Bayer Diagnostics Corp.11/14/2003SE
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K012301Immulite 2000 Digoxin, Models L2KDI2 (200 Tests) and L2KDI6 (600 Tests)KXT · Traditional Diagnostic Products Corp.09/19/2001SE
K011920Emit 2000 Digoxin Assay, Model OSR4H229KXT · Special Syva Co., Dade Behring, Inc.07/02/2001SE

More from Syva Co., Dade Behring, Inc.

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K914135Amerlite(Tm) PROLACTIN-30 Assay, LAN.0086/2086CFT · Traditional 02/18/1992SE
K912733Amerlex-M Specific Estrol(Unconjugated) Ria KitCIG · Traditional 07/22/1991SE
K912766Amerlite Ck-Mb AssayJHY · Traditional 07/17/1991SE
K904666Amerlite TSH-60 Assay Product Code: Lan. 0008/2008JLW · Traditional 11/02/1990SE
K902760Amersham TSH Control SeraJJX · Traditional 07/27/1990SE
K901857GADOLINIUM-153 Bone Densitometer (GDC.10413)KGI · Traditional 07/09/1990SE
K901854GADOLINIUM-153 Bone Densitometer (GDC.10411/10412)KGI · Traditional 07/09/1990SE
K901848GADOLINIUM-153 Bone Densitometer SourcesKGI · Traditional 07/09/1990SE
K901832GADOLINIUM-153 Bone Densitometer Sources GDC.10415KGI · Traditional 07/09/1990SE
K896270Amerlite ESTRADIOL-60 Assay LAN.0081/2081CHP · Traditional 12/12/1989SE

Questions and answers

When was Amerlite Digoxin Assay, LAN.0700/2700, 240/144 Kit cleared by the FDA?

Amerlite Digoxin Assay, LAN.0700/2700, 240/144 Kit (K880823) received a 510(k) decision of Substantially Equivalent on May 31, 1988, 91 days after the submission was received.

What is the product code of K880823?

The FDA product code is KXT – Enzyme Immunoassay, Digoxin, a Class II (moderate risk) device regulated under 21 CFR 862.3320.