Loci Vitamin B12 (VB12) Flex Reagent Cartridge, Loci Anemia Calibrator (Anem Cal)

FDA 510(k) K133512 · Siemens Healthcare Diagnostics

Substantially Equivalent

510(k) numberK133512

Submission

Device name
Loci Vitamin B12 (VB12) Flex Reagent Cartridge, Loci Anemia Calibrator (Anem Cal)
Applicant
Siemens Healthcare Diagnostics
Newark, DE, US
Received
November 15, 2013
Decision date
January 2, 2014
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 Loci Vitamin B12 (VB12) Flex Reagent Cartridge, Loci Anemia Calibrator (Anem Cal) cleared by the FDA?

Loci Vitamin B12 (VB12) Flex Reagent Cartridge, Loci Anemia Calibrator (Anem Cal) (K133512) received a 510(k) decision of Substantially Equivalent on January 2, 2014, 48 days after the submission was received.

What is the product code of K133512?

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