FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

SONOACE PICO DIAGNOSTIC ULTRASOUND SYSTEM

K Number: K061213 · Decision May 16, 2006
Classifications
1
FEI Numbers
211
Registration Numbers
211
Same Product Code
1117
Applicant Total
24
Review Days
14

Basic Information

Device Name
SONOACE PICO DIAGNOSTIC ULTRASOUND SYSTEM
K Number
K061213
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1550
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDISON CO., LTD.
Date Received
May 2, 2006
Decision Date
May 16, 2006
Product Code
IYN
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
IYN System, Imaging, Pulsed Doppler, Ultrasonic

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K101455 EKO 7 DIAGNOSTIC ULTRASOUND SYSTEM
K101829 THE SONOACE R3 DIAGNOSTIC ULTRASOUND SYSTEM
K100186 MYSONO U5 DIAGNOSTIC ULTRASOUND SYSTEM
K093849 ACCUVIX V10 DIAGNOSTIC ULTRASOUND SYSTEM
K093714 SONOACE X8 DIAGNOSTIC ULTRASOUND SYSTEM
K092159 ACCUVIX V20 DIAGNOSTIC ULTRASOUND SYSTEM
K081676 SONOACE X6 DIAGNOSTIC ULTRASOUND SYSTEM
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