Cleared Traditional

K102432 - DIAZYME 25-HYDROXY VITAMIN D ASSAY KIT MODEL DZ688A, DIAZYME 25-HYDROXY VITAMIN D ASSAY CALIBRATOR SET MODEL DZ688A-CAL, (FDA 510(k) Clearance)

Jan 2011
Decision
141d
Days
Class 2
Risk

K102432 is an FDA 510(k) clearance for the DIAZYME 25-HYDROXY VITAMIN D ASSAY KIT MODEL DZ688A, DIAZYME 25-HYDROXY VITAMIN D ASSAY CALIBRATOR SET MODEL DZ688A-CAL,. This device is classified as a System, Test, Vitamin D (Class II - Special Controls, product code MRG).

Submitted by Diazyme Laboratories (Poway, US). The FDA issued a Cleared decision on January 14, 2011, 141 days after receiving the submission on August 26, 2010.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1825.

Submission Details

510(k) Number K102432 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 26, 2010
Decision Date January 14, 2011
Days to Decision 141 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF

Device Classification

Product Code MRG — System, Test, Vitamin D
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.1825