NeoWave Pain Relief and Recovery System, Model# T16-2020— 510(k) K202693

Substantially Equivalent

Eva Medtec, Inc.

FDA 510(k) clearance K202693 for NeoWave Pain Relief and Recovery System, Model# T16-2020, Substantially Equivalent on 2021-03-05. Applicant: Eva Medtec, Inc..

Clearance details

Applicant: Eva Medtec, Inc.
Product code: Code IRP
Advisory panel: Physical Medicine
Date received: 2020-09-15
Decision date: 2021-03-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bloomington, MN, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.