Single Vial Lipase Test Kit

FDA 510(k) K802842 · Biodynamics Corp.

Substantially Equivalent

510(k) numberK802842

Submission

Device name
Single Vial Lipase Test Kit
Applicant
Biodynamics Corp.
Mchenry, IL, US
Received
November 12, 1980
Decision date
December 18, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CHI – Lipase-Esterase, Enzymatic, Photometric, Lipase
Device class
Class I (low risk)
Regulation
21 CFR 862.1465
Specialty
Clinical Chemistry

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K952180CX Lipase Reagent & Calibrator for Synchron CX SystemsCHI · Traditional Beckman Instruments, Inc.08/17/1995SE
K952816Lipase Flex Reagent CartridgeCHI · Traditional Dupont Medical Products07/20/1995SE
K952647Il Test LipaseCHI · Traditional Instrumentation Laboratory CO07/20/1995SE
K941085Lipase-Ps Assay Procedure No. 805CHI · Traditional Sigma Diagnostics, Inc.05/17/1994SE
K923917Elipase Human Pancreatic Lipase EnzymeimmunoassayCHI · Traditional Nuclear Diagnostics, Inc.02/25/1994SE
K921249Wako Autokit Lipase-ColorCHI · Traditional Wako Chemicals USA, Inc.07/21/1992SE
K920337Miles Lipase Sera-Pak MethodCHI · Traditional Heraeus Kulzer, Inc.03/11/1992SE
K900827Colorimetric Chloride Product #4314125CHI · Traditional American Research Products Co.05/02/1990SE

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Questions and answers

When was Single Vial Lipase Test Kit cleared by the FDA?

Single Vial Lipase Test Kit (K802842) received a 510(k) decision of Substantially Equivalent on December 18, 1980, 36 days after the submission was received.

What is the product code of K802842?

The FDA product code is CHI – Lipase-Esterase, Enzymatic, Photometric, Lipase, a Class I (low risk) device regulated under 21 CFR 862.1465.