Advia Chemistry GLUH_3 Reagents

FDA 510(k) K120681 · Siemens Healthcare Diagnostics, Inc.

Substantially Equivalent

510(k) numberK120681

Submission

Device name
Advia Chemistry GLUH_3 Reagents
Applicant
Siemens Healthcare Diagnostics, Inc.
Tarrytown, NY, US
Received
March 6, 2012
Decision date
May 15, 2012
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 Advia Chemistry GLUH_3 Reagents cleared by the FDA?

Advia Chemistry GLUH_3 Reagents (K120681) received a 510(k) decision of Substantially Equivalent on May 15, 2012, 70 days after the submission was received.

What is the product code of K120681?

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