VisiRad XR— 510(k) K223133

Substantially Equivalent

Imidex, Inc.

FDA 510(k) clearance K223133 for VisiRad XR, Substantially Equivalent on 2023-08-03. Applicant: Imidex, Inc..

Clearance details

Applicant: Imidex, Inc.
Product code: Code MYN
Advisory panel: Radiology
Date received: 2022-10-03
Decision date: 2023-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denver, CO, US

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