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MobileRay Pulse SE Digital Imaging System

Page Type
Cleared 510(K)
510(k) Number
K191503
510(k) Type
Traditional
Applicant
Portavision Medical LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/2019
Days to Decision
90 days
Submission Type
Summary

MobileRay Pulse SE Digital Imaging System

Page Type
Cleared 510(K)
510(k) Number
K191503
510(k) Type
Traditional
Applicant
Portavision Medical LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/2019
Days to Decision
90 days
Submission Type
Summary