Cleared Traditional

K142714 - S8 Exp/S9 Pro Portable Digital Color Do...

K142714 is an FDA 510(k) clearance for S8 Exp/S9 Pro Portable Digital Color Do..., manufactured by Sonoscape Company Limited. The device is a Class 2 Radiology device with product code IYN cleared through the Traditional 510(k) pathway after a 129-day FDA review.

K142714 · Sonoscape Company Limited · Radiology device
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Jan 2015
Decision
129d
Days
Class 2
Risk

K142714 is an FDA 510(k) clearance for the S8 Exp/S9 Pro Portable Digital Color Doppler Ultrasound System. Classified as System, Imaging, Pulsed Doppler, Ultrasonic within the IYN classification (a category covering pulsed Doppler and ultrasound imaging systems), Class II - Special Controls.

Submitted by Sonoscape Company Limited (Shenzhen, TW). The FDA issued a Cleared decision on January 29, 2015 after a review of 129 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1550 - the FDA radiology and imaging software oversight 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 Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Sonoscape Company Limited devices

FDA 510(k) Submission Details - K142714

510(k) Number K142714 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 22, 2014
Decision Date January 29, 2015
Days to Decision 129 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
22d slower than avg
Panel avg: 107d · This submission: 129d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IYN Device Classification - Class 2, Special Controls

Product Code IYN System, Imaging, Pulsed Doppler, Ultrasonic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1550
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 Radiology devices follow this clearance model.

Regulatory Peers - IYN System, Imaging, Pulsed Doppler, Ultrasonic

All 891
Devices cleared under the same product code (IYN) and FDA review panel - the closest regulatory comparables to K142714.
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LOGIQ P9, LOGIQ P7
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S22 Digital Color Doppler Ultrasound System
K142815 · Sonoscape Company Limited · Jan 2015
S9 Portable Digital Color Doppler Ultrasound System
K142710 · Sonoscape Company Limited · Jan 2015