QM300 Apolipoprotein A-I Antibody Pack

FDA 510(k) K883713 · Kallestad Diag, A Div. of Erbamont, Inc.

Substantially Equivalent

510(k) numberK883713

Submission

Device name
QM300 Apolipoprotein A-I Antibody Pack
Applicant
Kallestad Diag, A Div. of Erbamont, Inc.
Chaska, MN, US
Received
August 30, 1988
Decision date
October 19, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
MSJ – Apolipoproteins
Device class
Class I (low risk)
Regulation
21 CFR 862.1475
Specialty
Clinical Chemistry

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K061377Apolipoprotein A1 and Apolipoprotein B Reagents and CalibratorsMSJ · Traditional Pointe Scientific, Inc.,03/28/2007SE
K063608Dimension Vista APOA1 and Apob Flex Reagent Cartridges and Protein 1 Calibrator and…MSJ · Traditional Dade Behring, Inc.02/23/2007SE
K9926628 Additional Assays for the Bayer Advia 1650 Chemistry SystemMSJ · Traditional Bayer Corp.02/15/2000SE
K970314Synchron LX Systems Apolipoprotein (Apoa and Apob) ReagentsMSJ · Traditional Beckman Instruments, Inc.04/21/1997SE
K964010Immage Immunochemistry System Apolipoprotein A-1 Reagent (Apa)/ Immage Immunochemistry…MSJ · Traditional Beckman Instruments, Inc.02/10/1997SE
K931777Apo A-1 Chemiluminescence AssayMSJ · Traditional Nichols Institute08/16/1993SE
K925702Nichols Apo B Chemiluminescence AssayMSJ · Traditional Nichols Institute Diagnostics12/23/1992SE
K923087Il Test Apolipoprotein A1MSJ · Traditional Instrumentation Laboratory CO10/26/1992SE

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Questions and answers

When was QM300 Apolipoprotein A-I Antibody Pack cleared by the FDA?

QM300 Apolipoprotein A-I Antibody Pack (K883713) received a 510(k) decision of Substantially Equivalent on October 19, 1988, 50 days after the submission was received.

What is the product code of K883713?

The FDA product code is MSJ – Apolipoproteins, a Class I (low risk) device regulated under 21 CFR 862.1475.