Acs CKMB II Immunoassay

FDA 510(k) K962126 · Ciba Corning Diagnostics Corp.

Substantially Equivalent

510(k) numberK962126

Submission

Device name
Acs CKMB II Immunoassay
Applicant
Ciba Corning Diagnostics Corp.
Irvine, CA, US
Received
June 3, 1996
Decision date
June 21, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JHS – Differential Rate Kinetic Method, Cpk Or Isoenzymes
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1215
Specialty
Clinical Chemistry

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K062128The Dimension Vista Flex Reagent Cartridges / Kit AssaysJHS · Special Dade Behring, Inc.08/21/2006SE
K990439Careside CKJHS · Traditional Careside, Inc.04/19/1999SE
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K981495Immulite Ck-Mb, Catalog # LKCP1 (100 Tests), LKCP5 (500 Tests)JHS · Traditional Diagnostic Products Corp.06/10/1998SE
K952250Stratus Ck-Mb Dendrimer Fluorometric Enzyme Immunoassay & Stratus Ck-Mb Dendrimer High…JHS · Traditional Dade Intl., Inc.07/17/1995SE
K945083Access Ck-Mb ReagentsJHS · Traditional Bio-Rad Laboratories, Inc.11/21/1994SE
K943024Kinase IsoenzymeJHS · Traditional Dupont Medical Products08/02/1994SE

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Questions and answers

When was Acs CKMB II Immunoassay cleared by the FDA?

Acs CKMB II Immunoassay (K962126) received a 510(k) decision of Substantially Equivalent on June 21, 1996, 18 days after the submission was received.

What is the product code of K962126?

The FDA product code is JHS – Differential Rate Kinetic Method, Cpk Or Isoenzymes, a Class II (moderate risk) device regulated under 21 CFR 862.1215.