Last synced on 14 November 2025 at 11:06 pm

VidiStar HeartView

Page Type
Cleared 510(K)
510(k) Number
K152822
510(k) Type
Traditional
Applicant
VIDISTAR, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/2015
Days to Decision
58 days
Submission Type
Summary

VidiStar HeartView

Page Type
Cleared 510(K)
510(k) Number
K152822
510(k) Type
Traditional
Applicant
VIDISTAR, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/2015
Days to Decision
58 days
Submission Type
Summary