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CX50 VERSION 2.0 DIAGNOSTIC ULTRASOUND SYSTEM AND TRANSDUCERS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091804
510(k) Type
Traditional
Applicant
Philips Ultrasound, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/2009
Days to Decision
29 days
Submission Type
Summary

CX50 VERSION 2.0 DIAGNOSTIC ULTRASOUND SYSTEM AND TRANSDUCERS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091804
510(k) Type
Traditional
Applicant
Philips Ultrasound, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/2009
Days to Decision
29 days
Submission Type
Summary