Last synced on 14 November 2025 at 11:06 pm

Prelivia

Page Type
Cleared 510(K)
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)
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