Isotrak Amylase Test Amylase Isoenzyme

FDA 510(k) K853951 · Behring Diagnostics, Inc.

Substantially Equivalent

510(k) numberK853951

Submission

Device name
Isotrak Amylase Test Amylase Isoenzyme
Applicant
Behring Diagnostics, Inc.
La Jolla, CA, US
Received
September 25, 1985
Decision date
January 7, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CIJ – Saccharogenic, Amylase
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1070
Specialty
Clinical Chemistry

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K980013AmylaseCIJ · Traditional Ac Biochemicals, Inc.02/04/1998SE
K953211Amylase (Ethylidene PNGPG7) KitCIJ · Traditional Randox Laboratories, Ltd.06/21/1996SE
K951494Amylase Test Item 97381/94 (R1, 97382/94 (R2-SR)CIJ · Traditional Emd Chemicals, Inc.12/11/1995SE
K940735Liquid Amylase (CNPG3) Reagent SetCIJ · Traditional Pointe Scientific, Inc.,08/01/1994SE
K940010Dma Amylase (Demand) ProcedureCIJ · Traditional Data Medical Associates, Inc.03/11/1994SE
K931301Olympus Amylase ReagentCIJ · Traditional Olympus Corp.10/18/1993SE
K931141Biotrol Amylase CNPG3CIJ · Traditional Biotrol, USA, Inc.05/26/1993SE
K882225-Amylase EpsCIJ · Traditional Boehringer Mannheim Corp.01/03/1989SE

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Questions and answers

When was Isotrak Amylase Test Amylase Isoenzyme cleared by the FDA?

Isotrak Amylase Test Amylase Isoenzyme (K853951) received a 510(k) decision of Substantially Equivalent on January 7, 1986, 104 days after the submission was received.

What is the product code of K853951?

The FDA product code is CIJ – Saccharogenic, Amylase, a Class II (moderate risk) device regulated under 21 CFR 862.1070.