Cleared Traditional

K013327 - CTS-415

K013327 is an FDA 510(k) clearance for CTS-415, manufactured by Shantou Institute of Ultrasonic Instuments. The device is a Class 2 Radiology device with product code IYO cleared through the Traditional 510(k) pathway after a 70-day FDA review.

K013327 · Shantou Institute of Ultrasonic Instuments · Radiology device
Download Printable Device Report (PDF)
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Dec 2001
Decision
70d
Days
Class 2
Risk

K013327 is an FDA 510(k) clearance for the CTS-415. Classified as System, Imaging, Pulsed Echo, Ultrasonic (product code IYO), Class II - Special Controls.

Submitted by Shantou Institute of Ultrasonic Instuments (Walnut Creek, US). The FDA issued a Cleared decision on December 14, 2001 after a review of 70 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1560 - 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: 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 Shantou Institute of Ultrasonic Instuments devices

FDA 510(k) Submission Details - K013327

510(k) Number K013327 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 05, 2001
Decision Date December 14, 2001
Days to Decision 70 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
37d faster than avg
Panel avg: 107d · This submission: 70d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IYO Device Classification - Class 2, Special Controls

Product Code IYO System, Imaging, Pulsed Echo, Ultrasonic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1560
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 - IYO System, Imaging, Pulsed Echo, Ultrasonic

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