Prelivia— 510(k) K210979

Substantially Equivalent

Rehabtronics, Inc.

FDA 510(k) clearance K210979 for Prelivia, Substantially Equivalent on 2021-05-13. Applicant: Rehabtronics, Inc..

Clearance details

Applicant: Rehabtronics, Inc.
Product code: Code IPF
Advisory panel: Physical Medicine
Date received: 2021-04-01
Decision date: 2021-05-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Edmonton, CA

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