Elecsys Vitamin B12 II assay, Elecsys Vitamin B12 II CalSet

FDA 510(k) K151786 · Roche Diagnostics

Substantially Equivalent

510(k) numberK151786

Submission

Device name
Elecsys Vitamin B12 II assay, Elecsys Vitamin B12 II CalSet
Applicant
Roche Diagnostics
Indianapolis, IN, US
Received
July 1, 2015
Decision date
September 24, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CDD – Radioassay, Vitamin B12
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1810
Specialty
Clinical Chemistry

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Questions and answers

When was Elecsys Vitamin B12 II assay, Elecsys Vitamin B12 II CalSet cleared by the FDA?

Elecsys Vitamin B12 II assay, Elecsys Vitamin B12 II CalSet (K151786) received a 510(k) decision of Substantially Equivalent on September 24, 2015, 85 days after the submission was received.

What is the product code of K151786?

The FDA product code is CDD – Radioassay, Vitamin B12, a Class II (moderate risk) device regulated under 21 CFR 862.1810.