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Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K212704
510(k) Type
Traditional
Applicant
Philips Medical Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/24/2021
Days to Decision
29 days
Submission Type
Summary

Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K212704
510(k) Type
Traditional
Applicant
Philips Medical Systems
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/24/2021
Days to Decision
29 days
Submission Type
Summary