Bacton(Tm), Auto-Apo B Reagent

FDA 510(k) K921862 · Bacton Assay Systems, Inc.

Substantially Equivalent

510(k) numberK921862

Submission

Device name
Bacton(Tm), Auto-Apo B Reagent
Applicant
Bacton Assay Systems, Inc.
San Marcos, CA, US
Received
April 14, 1992
Decision date
June 22, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

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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K072977Diazyme Apolipoprotein A-1 AssayMSJ · Traditional General Atomics07/16/2008SE
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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

More from Instrumentation Laboratory CO

510(k)DeviceDecision
K921795Bacton(Tm), Auto-Apo A-1 ReagentMSJ · Traditional 06/23/1992SE

Questions and answers

When was Bacton(Tm), Auto-Apo B Reagent cleared by the FDA?

Bacton(Tm), Auto-Apo B Reagent (K921862) received a 510(k) decision of Substantially Equivalent on June 22, 1992, 69 days after the submission was received.

What is the product code of K921862?

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