Last synced on 19 July 2024 at 11:05 pm

Relivion

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212106
510(k) Type
Special
Applicant
Neurolief Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/2/2021
Days to Decision
27 days
Submission Type
Summary

Relivion

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212106
510(k) Type
Special
Applicant
Neurolief Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/2/2021
Days to Decision
27 days
Submission Type
Summary