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

ViewPoint 6

K Number: K203677 · Decision Jan 15, 2021
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
14
Review Days
29

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Basic Information

Device Name
ViewPoint 6
K Number
K203677
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC
Date Received
December 17, 2020
Decision Date
January 15, 2021
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

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