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PercuNav Image Fusion and Interventional Navigation System

Page Type
Cleared 510(K)
510(k) Number
K223804
510(k) Type
Traditional
Applicant
Philips Ultrasound LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2023
Days to Decision
30 days
Submission Type
Summary

PercuNav Image Fusion and Interventional Navigation System

Page Type
Cleared 510(K)
510(k) Number
K223804
510(k) Type
Traditional
Applicant
Philips Ultrasound LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2023
Days to Decision
30 days
Submission Type
Summary