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

Acuson SC2000 Diagnostic Ultrasound System

K Number: K171766 · Decision Jul 12, 2017
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
32
Review Days
28

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Basic Information

Device Name
Acuson SC2000 Diagnostic Ultrasound System
K Number
K171766
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Siemens Medi Cal Solutions, Inc.
Date Received
June 14, 2017
Decision Date
July 12, 2017
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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