Cleared Traditional

K142800 - Rapid Single/Multi-drug Test Cup and Rapid Single/Multi-drug Test Dipcard

K142800 is an FDA 510(k) clearance for Rapid Single/Multi-drug Test Cup and Ra..., manufactured by Co-Innovation Biotech Co., Ltd.. The device is a Class 2 Toxicology device with product code DKZ cleared through the Traditional 510(k) pathway after a 73-day FDA review.

K142800 · Co-Innovation Biotech Co., Ltd. · Toxicology device
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Dec 2014
Decision
73d
Days
Class 2
Risk

K142800 is an FDA 510(k) clearance for the Rapid Single/Multi-drug Test Cup and Rapid Single/Multi-drug Test Dipcard. Classified as Enzyme Immunoassay, Amphetamine (product code DKZ), Class II - Special Controls.

Submitted by Co-Innovation Biotech Co., Ltd. (Guangzhou, CN). The FDA issued a Cleared decision on December 11, 2014 after a review of 73 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.3100 - the FDA toxicology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Co-Innovation Biotech Co., Ltd. devices

FDA 510(k) Submission Details - K142800

510(k) Number K142800 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 29, 2014
Decision Date December 11, 2014
Days to Decision 73 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
14d faster than avg
Panel avg: 87d · This submission: 73d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DKZ Device Classification - Class 2, Special Controls

Product Code DKZ Enzyme Immunoassay, Amphetamine
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.3100
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 Toxicology devices follow this clearance model.

Regulatory Peers - DKZ Enzyme Immunoassay, Amphetamine

All 208
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