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EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243793
510(k) Type
Traditional
Applicant
Philips Ultrasound LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2025
Days to Decision
162 days
Submission Type
Summary

EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243793
510(k) Type
Traditional
Applicant
Philips Ultrasound LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2025
Days to Decision
162 days
Submission Type
Summary