Ace Alera Clinical Chemistry System, Ace Glucose Reagent, Ace Ion Selective Electrode (Ise) Module

FDA 510(k) K123018 · Alfa Wassermann Diagnostic Technologies, Inc.

Substantially Equivalent

510(k) numberK123018

Submission

Device name
Ace Alera Clinical Chemistry System, Ace Glucose Reagent, Ace Ion Selective Electrode (Ise) Module
Applicant
Alfa Wassermann Diagnostic Technologies, Inc.
West Caldwell, NJ, US
Received
September 28, 2012
Decision date
April 23, 2013
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CFR – Hexokinase, Glucose
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1345
Specialty
Clinical Chemistry

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Questions and answers

When was Ace Alera Clinical Chemistry System, Ace Glucose Reagent, Ace Ion Selective Electrode (Ise) Module cleared by the FDA?

Ace Alera Clinical Chemistry System, Ace Glucose Reagent, Ace Ion Selective Electrode (Ise) Module (K123018) received a 510(k) decision of Substantially Equivalent on April 23, 2013, 207 days after the submission was received.

What is the product code of K123018?

The FDA product code is CFR – Hexokinase, Glucose, a Class II (moderate risk) device regulated under 21 CFR 862.1345.