Last synced on 25 January 2026 at 3:41 am

Prelivia

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210979
510(k) Type
Traditional
Applicant
Rehabtronics, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/13/2021
Days to Decision
42 days
Submission Type
Statement

Prelivia

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210979
510(k) Type
Traditional
Applicant
Rehabtronics, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/13/2021
Days to Decision
42 days
Submission Type
Statement