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EPIQ Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K200304
510(k) Type
Traditional
Applicant
Philips Ultrasound, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2020
Days to Decision
29 days
Submission Type
Summary

EPIQ Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K200304
510(k) Type
Traditional
Applicant
Philips Ultrasound, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/6/2020
Days to Decision
29 days
Submission Type
Summary