Atac Pak Albumin Reagent

FDA 510(k) K030006 · Elan Diagnostics

Substantially Equivalent

510(k) numberK030006

Submission

Device name
Atac Pak Albumin Reagent
Applicant
Elan Diagnostics
Brea, CA, US
Received
January 2, 2003
Decision date
March 7, 2003
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CIX – Bromcresol Green Dye-Binding, Albumin
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1035
Specialty
Clinical Chemistry

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More from Medica Corp.

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K030003Atac Direct Bilirubin Reagent and CalibratorCIG · Traditional 09/29/2003SE
K030014Atac Total Bilirubin ReagentCIG · Traditional 09/26/2003SE
K030621Atac CalibratorJIX · Traditional 03/19/2003SE
K023105Atac Calcium Reagent and Atac CalibratorCIC · Traditional 03/13/2003SE
K030010Atac Pak Magnesium ReagentJGJ · Traditional 03/10/2003SE
K030015Atac Pak Phosphorus ReagentCEO · Traditional 03/07/2003SE
K023407Atac Pak Creatinine Reagent and Atac CalibratorCGX · Traditional 02/14/2003SE
K021385Atac Pak Bun ReagentCDQ · Traditional 07/12/2002SE
K020575Atac Direct LDL Reagent and Atac Direct LDL Calibrator KitsMRR · Traditional 04/12/2002SE
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Questions and answers

When was Atac Pak Albumin Reagent cleared by the FDA?

Atac Pak Albumin Reagent (K030006) received a 510(k) decision of Substantially Equivalent on March 7, 2003, 64 days after the submission was received.

What is the product code of K030006?

The FDA product code is CIX – Bromcresol Green Dye-Binding, Albumin, a Class II (moderate risk) device regulated under 21 CFR 862.1035.