Dimension Vista Albumin, Alkaline Phosphatase, Aspartate Amino Transferase, Carbamazepine & Alanine Amino Transferase

FDA 510(k) K061020 · Dade Behring, Inc.

Substantially Equivalent

510(k) numberK061020

Submission

Device name
Dimension Vista Albumin, Alkaline Phosphatase, Aspartate Amino Transferase, Carbamazepine & Alanine Amino Transferase
Applicant
Dade Behring, Inc.
Newark, DE, US
Received
April 13, 2006
Decision date
May 10, 2006
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CKA – Nadh Oxidation/Nad Reduction, Alt/Sgpt
Device class
Class I (low risk)
Regulation
21 CFR 862.1030
Specialty
Clinical Chemistry

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Questions and answers

When was Dimension Vista Albumin, Alkaline Phosphatase, Aspartate Amino Transferase, Carbamazepine & Alanine Amino Transferase cleared by the FDA?

Dimension Vista Albumin, Alkaline Phosphatase, Aspartate Amino Transferase, Carbamazepine & Alanine Amino Transferase (K061020) received a 510(k) decision of Substantially Equivalent on May 10, 2006, 27 days after the submission was received.

What is the product code of K061020?

The FDA product code is CKA – Nadh Oxidation/Nad Reduction, Alt/Sgpt, a Class I (low risk) device regulated under 21 CFR 862.1030.