Last synced on 14 November 2025 at 11:06 pm

EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K250177
510(k) Type
Traditional
Applicant
Philips Ultrasound LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/2025
Days to Decision
78 days
Submission Type
Summary

EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K250177
510(k) Type
Traditional
Applicant
Philips Ultrasound LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/2025
Days to Decision
78 days
Submission Type
Summary