Cleared Traditional

K103557 - DIAZYME HS CRP ASSAY KIT / CALIBRATOR S...

K103557 is an FDA 510(k) clearance for DIAZYME HS CRP ASSAY KIT / CALIBRATOR S..., manufactured by Diazyme Laboratories. The device is a Class 2 Chemistry device with product code DCK cleared through the Traditional 510(k) pathway after a 146-day FDA review.

K103557 · Diazyme Laboratories · Chemistry device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
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. Classified as C-reactive Protein, Antigen, Antiserum, And Control (product code DCK), Class II - Special Controls.

Submitted by Diazyme Laboratories (Poway, US). The FDA issued a Cleared decision on April 27, 2011 after a review of 146 days - within the typical 510(k) review window.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 866.5270 - the FDA in vitro diagnostics and chemistry framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Chemistry review framework, consistent with the majority of Class II 510(k) submissions.

View all Diazyme Laboratories devices

FDA 510(k) Submission Details - K103557

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
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
58d slower than avg
Panel avg: 88d · This submission: 146d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DCK Device Classification - Class 2, Special Controls

Product Code DCK C-reactive Protein, Antigen, Antiserum, And Control
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.5270
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - DCK C-reactive Protein, Antigen, Antiserum, And Control

All 94
Devices cleared under the same product code (DCK) and FDA review panel - the closest regulatory comparables to K103557.
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ABX PENTRA 400 : CRP
K061138 · Horiba Abx · Sep 2006
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K060139 · Diagnostic Chemicals , Ltd. · Apr 2006
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K052591 · Clinical Data, Inc. · Feb 2006