Vitamin D Test System Nichols Advantage 25-HYDROXYVITAMIN D

FDA 510(k) K012367 · Nichols Institute Diagnostics

Substantially Equivalent

510(k) numberK012367

Submission

Device name
Vitamin D Test System Nichols Advantage 25-HYDROXYVITAMIN D
Applicant
Nichols Institute Diagnostics
San Juan Capistrano, CA, US
Received
July 26, 2001
Decision date
October 9, 2001
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JIT – Calibrator, Secondary
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1150
Specialty
Clinical Chemistry

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Questions and answers

When was Vitamin D Test System Nichols Advantage 25-HYDROXYVITAMIN D cleared by the FDA?

Vitamin D Test System Nichols Advantage 25-HYDROXYVITAMIN D (K012367) received a 510(k) decision of Substantially Equivalent on October 9, 2001, 75 days after the submission was received.

What is the product code of K012367?

The FDA product code is JIT – Calibrator, Secondary, a Class II (moderate risk) device regulated under 21 CFR 862.1150.