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

ARIETTA 60/ARIETTAS60/ARIETTAV60

K Number: K140443 · Decision Jun 16, 2014
Classifications
1
FEI Numbers
220
Registration Numbers
220
Same Product Code
1171
Applicant Total
3
Review Days
115

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Basic Information

Device Name
ARIETTA 60/ARIETTAS60/ARIETTAV60
K Number
K140443
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1550
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hitachi Aloka Medical,Ltd. (Hitachi Aloka Medical
Date Received
February 21, 2014
Decision Date
June 16, 2014
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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Other Clearances by Hitachi Aloka Medical,Ltd. (Hitachi Aloka Medical

K Number Device Name
K134016 ARIETTA 70/ARIETTA S70/ARIETTA V70 DIAGNOSTIC ULTRASOUND SCANNER
K122537 PROUSOUND ALPHA 7 VER. 6.0 DIAGNOSTIC ULTRASOUND SYSTEM MODEL: PROSOUND ALPHA 7 VER. 6.0