Advia Chemistry Cardiophase High Sensitivity C-Reactive Protein (Hscrp), Calibrators

FDA 510(k) K081294 · Siemens Healthcare Diagnostics, Inc.

Substantially Equivalent

510(k) numberK081294

Submission

Device name
Advia Chemistry Cardiophase High Sensitivity C-Reactive Protein (Hscrp), Calibrators
Applicant
Siemens Healthcare Diagnostics, Inc.
Tarrytown, NY, US
Received
May 7, 2008
Decision date
July 29, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NQD – Cardiac C-Reactive Protein, Antigen, Antiserum, And Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5270
Specialty
Immunology

In vitro diagnostic test to measure C-reactive protein for the purpose of making cardiac risk assessments.

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Questions and answers

When was Advia Chemistry Cardiophase High Sensitivity C-Reactive Protein (Hscrp), Calibrators cleared by the FDA?

Advia Chemistry Cardiophase High Sensitivity C-Reactive Protein (Hscrp), Calibrators (K081294) received a 510(k) decision of Substantially Equivalent on July 29, 2008, 83 days after the submission was received.

What is the product code of K081294?

The FDA product code is NQD – Cardiac C-Reactive Protein, Antigen, Antiserum, And Control, a Class II (moderate risk) device regulated under 21 CFR 866.5270.