FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

A6 PORTABLE ULTRASONIC DIAGNOSTIC SYSTEM

K Number: K101337 · Decision Sep 30, 2010
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
22
Review Days
141

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Basic Information

Device Name
A6 PORTABLE ULTRASONIC DIAGNOSTIC SYSTEM
K Number
K101337
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sonoscape Company Limited
Date Received
May 12, 2010
Decision Date
September 30, 2010
Product Code
IYO
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

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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K131262 DIGITAL ELECTROCARDIOGRAPHS
K132527 DIGITAL COLOR DOPPLER ULTASOUND SYSTEM
K132768 S8 EXP PORTABLE DIGITAL COLOR DOPPLER ULTRASOUND SYSTEM
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