Vitros Immunodiagnostic Products 25-OH Vitamin D Total Reagent Pack, Vitamin D Total Calibrators

FDA 510(k) K121608 · Ortho-Clinical Diagnostics, Inc.

Substantially Equivalent

510(k) numberK121608

Submission

Device name
Vitros Immunodiagnostic Products 25-OH Vitamin D Total Reagent Pack, Vitamin D Total Calibrators
Applicant
Ortho-Clinical Diagnostics, Inc.
Rochester, NY, US
Received
June 1, 2012
Decision date
February 15, 2013
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MRG – System, Test, Vitamin D
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1825
Specialty
Clinical Chemistry

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Questions and answers

When was Vitros Immunodiagnostic Products 25-OH Vitamin D Total Reagent Pack, Vitamin D Total Calibrators cleared by the FDA?

Vitros Immunodiagnostic Products 25-OH Vitamin D Total Reagent Pack, Vitamin D Total Calibrators (K121608) received a 510(k) decision of Substantially Equivalent on February 15, 2013, 259 days after the submission was received.

What is the product code of K121608?

The FDA product code is MRG – System, Test, Vitamin D, a Class II (moderate risk) device regulated under 21 CFR 862.1825.