Last synced on 19 July 2024 at 11:05 pm

Vesseal

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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