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

S6 DIAGNOSTIC ULTRASOUND SYSTEM

K Number: K112602 · Decision Nov 7, 2011
Classifications
1
FEI Numbers
211
Registration Numbers
211
Same Product Code
1117
Applicant Total
22
Review Days
61

Basic Information

Device Name
S6 DIAGNOSTIC ULTRASOUND SYSTEM
K Number
K112602
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1550
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SONOSCAPE COMPANY LIMITED
Date Received
September 7, 2011
Decision Date
November 7, 2011
Product Code
IYN
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
IYN System, Imaging, Pulsed Doppler, Ultrasonic

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