Cleared Traditional

K033056 - BUN REAGENT FOR BECKMAN SYNCHRON CX & C...

K033056 is an FDA 510(k) clearance for BUN REAGENT FOR BECKMAN SYNCHRON CX & C..., manufactured by Diamond Diagnostics, Inc.. The device is a Class 2 Chemistry device with product code CDS cleared through the Traditional 510(k) pathway after a 123-day FDA review.

K033056 · Diamond Diagnostics, Inc. · Chemistry device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 2004
Decision
123d
Days
Class 2
Risk

K033056 is an FDA 510(k) clearance for the BUN REAGENT FOR BECKMAN SYNCHRON CX & CX DELTA REAGENT. Classified as Electrode, Ion Specific, Urea Nitrogen (product code CDS), Class II - Special Controls.

Submitted by Diamond Diagnostics, Inc. (Holliston, US). The FDA issued a Cleared decision on January 30, 2004 after a review of 123 days - within the typical 510(k) review window.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1770 - 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 Diamond Diagnostics, Inc. devices

FDA 510(k) Submission Details - K033056

510(k) Number K033056 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 29, 2003
Decision Date January 30, 2004
Days to Decision 123 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
35d slower than avg
Panel avg: 88d · This submission: 123d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

CDS Device Classification - Class 2, Special Controls

Product Code CDS Electrode, Ion Specific, Urea Nitrogen
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1770
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 - CDS Electrode, Ion Specific, Urea Nitrogen

All 8
Devices cleared under the same product code (CDS) and FDA review panel - the closest regulatory comparables to K033056.
epoc Blood Urea Nitrogen Test, epoc Total Carbon Dioxide Test
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