Cleared Traditional

K103557 - DIAZYME HS CRP ASSAY KIT / CALIBRATOR SET / CONTROL SET (FDA 510(k) Clearance)

Apr 2011
Decision
146d
Days
Class 2
Risk

K103557 is an FDA 510(k) clearance for the DIAZYME HS CRP ASSAY KIT / CALIBRATOR SET / CONTROL SET. This device is classified as a C-reactive Protein, Antigen, Antiserum, And Control (Class II - Special Controls, product code DCK).

Submitted by Diazyme Laboratories (Poway, US). The FDA issued a Cleared decision on April 27, 2011, 146 days after receiving the submission on December 2, 2010.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 866.5270.

Submission Details

510(k) Number K103557 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 02, 2010
Decision Date April 27, 2011
Days to Decision 146 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF

Device Classification

Product Code DCK — C-reactive Protein, Antigen, Antiserum, And Control
Device Class Class II - Special Controls
CFR Regulation 21 CFR 866.5270