Kinetic 610 Ethanol

FDA 510(k) K872180 · American Monitor Corp.

Substantially Equivalent

510(k) numberK872180

Submission

Device name
Kinetic 610 Ethanol
Applicant
American Monitor Corp.
Indianapolis, IN, US
Received
June 8, 1987
Decision date
July 7, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DML – Nad-Nadh, Specific Reagent For Alcohol Enzyme Method
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3040
Specialty
Clinical Toxicology

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K963197On.Site AlcoholDML · Traditional Ansys, Inc.09/19/1996SE
K953765Axsym Rea EthanolDML · Traditional Abbott Laboratories09/27/1995SE
K952839Boehringer Mannheim Ethyl Alcohol AssayDML · Traditional Boehringer Mannheim Corp.08/24/1995SE
K923337On*Site AlcoholDML · Traditional Toxi-Lab, Inc.01/12/1993SE
K914777Sigma Procedure No. 333-UVDML · Traditional Sigma Diagnostics, Inc.12/27/1991SE
K874382Raichem(Tm) Alcohol ReagentDML · Traditional Reagents Applications, Inc.01/11/1988SE
K863419Emds(Tm) Alcohol Testpacks, #67691/95DML · Traditional Em Diagnostic Systems, Inc.09/29/1986SE
K840769Paramax Alcohol ReagentDML · Traditional American Dade04/13/1984SE

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Questions and answers

When was Kinetic 610 Ethanol cleared by the FDA?

Kinetic 610 Ethanol (K872180) received a 510(k) decision of Substantially Equivalent on July 7, 1987, 29 days after the submission was received.

What is the product code of K872180?

The FDA product code is DML – Nad-Nadh, Specific Reagent For Alcohol Enzyme Method, a Class II (moderate risk) device regulated under 21 CFR 862.3040.