Sentinel Lipase Liquid Model 17.401B

FDA 510(k) K961179 · Equal Diagnostics, Inc.

Substantially Equivalent

510(k) numberK961179

Submission

Device name
Sentinel Lipase Liquid Model 17.401B
Applicant
Equal Diagnostics, Inc.
Exton, PA, US
Received
March 26, 1996
Decision date
July 19, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

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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K952816Lipase Flex Reagent CartridgeCHI · Traditional Dupont Medical Products07/20/1995SE
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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
K897150Lipase Color [Toyo] Serum Lipase Test KitCHI · Traditional Toyo Jozo Co., Ltd.02/26/1990SE

More from Toyo Jozo Co., Ltd.

510(k)DeviceDecision
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Questions and answers

When was Sentinel Lipase Liquid Model 17.401B cleared by the FDA?

Sentinel Lipase Liquid Model 17.401B (K961179) received a 510(k) decision of Substantially Equivalent on July 19, 1996, 115 days after the submission was received.

What is the product code of K961179?

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