Il 35260, Il Test Amylase Reagent

FDA 510(k) K873572 · Instrumentation Laboratory CO

Substantially Equivalent

510(k) numberK873572

Submission

Device name
Il 35260, Il Test Amylase Reagent
Applicant
Instrumentation Laboratory CO
Lexington, MA, US
Received
September 2, 1987
Decision date
October 20, 1987
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

Other 510(k)s with product code CIJ

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K023396Amylase EPS-G7 (Liquid) Reagent Set, (Hitachi Analyzers)CIJ · Traditional Pointe Scientific, Inc.,12/23/2002SE
K991817Additional Ims Assays for the Bayer Advia Ims SystemCIJ · Traditional Bayer Corp.07/22/1999SE
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 Il 35260, Il Test Amylase Reagent cleared by the FDA?

Il 35260, Il Test Amylase Reagent (K873572) received a 510(k) decision of Substantially Equivalent on October 20, 1987, 48 days after the submission was received.

What is the product code of K873572?

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