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VASOBand Vascular Compression Device

Page Type
Cleared 510(K)
510(k) Number
K203803
510(k) Type
Traditional
Applicant
VASOInnovations, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/2021
Days to Decision
29 days
Submission Type
Summary

VASOBand Vascular Compression Device

Page Type
Cleared 510(K)
510(k) Number
K203803
510(k) Type
Traditional
Applicant
VASOInnovations, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/2021
Days to Decision
29 days
Submission Type
Summary