Cleared Traditional

K140809 - CLIQ DV-300 ASPIRATOR

K140809 is an FDA 510(k) clearance for CLIQ DV-300 ASPIRATOR, manufactured by Ding Hwa Co., Ltd.. The device is a Class 2 General & Plastic Surgery device with product code JCX cleared through the Traditional 510(k) pathway after a 83-day FDA review.

K140809 · Ding Hwa Co., Ltd. · General & Plastic Surgery device
Download Printable Device Report (PDF)
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Jun 2014
Decision
83d
Days
Class 2
Risk

K140809 is an FDA 510(k) clearance for the CLIQ DV-300 ASPIRATOR. Classified as Apparatus, Suction, Ward Use, Portable, Ac-powered (product code JCX), Class II - Special Controls.

Submitted by Ding Hwa Co., Ltd. (Alpharetta, US). The FDA issued a Cleared decision on June 23, 2014 after a review of 83 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4780 - the FDA general and plastic surgery 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 Ding Hwa Co., Ltd. devices

FDA 510(k) Submission Details - K140809

510(k) Number K140809 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 01, 2014
Decision Date June 23, 2014
Days to Decision 83 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
32d faster than avg
Panel avg: 115d · This submission: 83d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JCX Device Classification - Class 2, Special Controls

Product Code JCX Apparatus, Suction, Ward Use, Portable, Ac-powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4780
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 General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - JCX Apparatus, Suction, Ward Use, Portable, Ac-powered

All 29
Devices cleared under the same product code (JCX) and FDA review panel - the closest regulatory comparables to K140809.
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