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Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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