Hitachi Clinical Analyzer S Test Reagent Cartridges for LD and Amy

FDA 510(k) K130685 · Hitachi Chemical Diagnostics, Inc.

Substantially Equivalent

510(k) numberK130685

Submission

Device name
Hitachi Clinical Analyzer S Test Reagent Cartridges for LD and Amy
Applicant
Hitachi Chemical Diagnostics, Inc.
Los Angeles, CA, US
Received
March 13, 2013
Decision date
August 9, 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
JFJ – Catalytic Methods, Amylase
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1070
Specialty
Clinical Chemistry

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Questions and answers

When was Hitachi Clinical Analyzer S Test Reagent Cartridges for LD and Amy cleared by the FDA?

Hitachi Clinical Analyzer S Test Reagent Cartridges for LD and Amy (K130685) received a 510(k) decision of Substantially Equivalent on August 9, 2013, 149 days after the submission was received.

What is the product code of K130685?

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