Revi System— 510(k) DEN220073

Unknown

Bluewind Medical , Ltd.

FDA 510(k) clearance DEN220073 for Revi System, Unknown on 2023-08-16. Applicant: Bluewind Medical , Ltd..

Clearance details

Applicant: Bluewind Medical , Ltd.
Product code: Code QXM
Advisory panel: Gastroenterology, Urology
Date received: 2022-10-05
Decision date: 2023-08-16
Decision: Unknown
Clearance type: Direct
Location: Herzliya, IL

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