Extended Range HS CRP Kit, Cat NO:9200

FDA 510(k) K030044 · Reference Diagnostics, Inc.

Substantially Equivalent

510(k) numberK030044

Submission

Device name
Extended Range HS CRP Kit, Cat NO:9200
Applicant
Reference Diagnostics, Inc.
Bedford, MA, US
Received
January 6, 2003
Decision date
September 30, 2003
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

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

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Questions and answers

When was Extended Range HS CRP Kit, Cat NO:9200 cleared by the FDA?

Extended Range HS CRP Kit, Cat NO:9200 (K030044) received a 510(k) decision of Substantially Equivalent on September 30, 2003, 267 days after the submission was received.

What is the product code of K030044?

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