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

FLYING DIAGNOSTIC ULTRASOUND SYSTEM

K Number: K083877 · Decision Jan 13, 2009
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
23
Review Days
15

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Basic Information

Device Name
FLYING DIAGNOSTIC ULTRASOUND SYSTEM
K Number
K083877
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Neusoft Medical Systems Co., Ltd.
Date Received
December 29, 2008
Decision Date
January 13, 2009
Product Code
ITX
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
ITX Transducer, Ultrasonic, Diagnostic

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K133373 CLEARVIEW
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