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SiteSeal Femoral Compression Device

Page Type
Cleared 510(K)
510(k) Number
K192413
510(k) Type
Traditional
Applicant
Ensite Vacular, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2020
Days to Decision
209 days
Submission Type
Summary

SiteSeal Femoral Compression Device

Page Type
Cleared 510(K)
510(k) Number
K192413
510(k) Type
Traditional
Applicant
Ensite Vacular, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2020
Days to Decision
209 days
Submission Type
Summary