Last synced on 14 November 2025 at 11:06 pm

CX50 VERSION 2.0 DIAGNOSTIC ULTRASOUND SYSTEM AND TRANSDUCERS

Page Type
Cleared 510(K)
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)
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