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EPIQ Series Diagnostic Ultrasound Systems

Page Type
Cleared 510(K)
510(k) Number
K202216
510(k) Type
Traditional
Applicant
Philips Ultrasound, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2020
Days to Decision
27 days
Submission Type
Summary

EPIQ Series Diagnostic Ultrasound Systems

Page Type
Cleared 510(K)
510(k) Number
K202216
510(k) Type
Traditional
Applicant
Philips Ultrasound, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/2/2020
Days to Decision
27 days
Submission Type
Summary