FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CTS-415

K Number: K013327 · Decision Dec 14, 2001
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
11
Review Days
70

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Basic Information

Device Name
CTS-415
K Number
K013327
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shantou Institute of Ultrasonic Instuments
Date Received
October 5, 2001
Decision Date
December 14, 2001
Product Code
IYO
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IYO System, Imaging, Pulsed Echo, Ultrasonic

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Other Clearances by Shantou Institute of Ultrasonic Instuments

K Number Device Name
K113613 DIGITAL COLOR DOPPLER ULTRASOUND IMAGING SYSTEM
K092907 DIGITAL ULTRASOUND IMAGING SYSTEM, CONVEX ARRAY TRANSDUCER, LINEAR ARRAY TRANSDUCER, CONVEX ARRAY TRANSDUCER, PHASED ARR
K081110 SIUI CTS-900 DIGITAL ULTRASOUND IMAGING SYSTEM
K070982 CTS-7700 DIGITAL ULTRASOUND IMAGING SYSTEM
K061083 CTS-7700
K012772 CTS-485 ULTRASOUND IMAGING SYSTEM
K984203 SIUI APOGEE 800PLUS ULTRASOUND IMAGING SYSTEM
K984161 CTS-310(B)
K963065 CTS-285 WITH EZU-PL21 AND EZU-PC3B TRANSDUCERS
K963068 CTS-200 WITH EZU-PL21 TRANSDUCER
Search all 11 clearances from Shantou Institute of Ultrasonic Instuments →