Last synced on 14 November 2025 at 11:06 pm

Vesseal

Page Type
Cleared 510(K)
510(k) Number
K221280
510(k) Type
Traditional
Applicant
Lydus Medical Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
12/9/2022
Days to Decision
220 days
Submission Type
Summary

Vesseal

Page Type
Cleared 510(K)
510(k) Number
K221280
510(k) Type
Traditional
Applicant
Lydus Medical Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
12/9/2022
Days to Decision
220 days
Submission Type
Summary