Enlight 2100— 510(k) K222897

Substantially Equivalent

Timpel S.A.

FDA 510(k) clearance K222897 for Enlight 2100, Substantially Equivalent on 2023-03-07. Applicant: Timpel S.A..

Clearance details

Applicant: Timpel S.A.
Product code: Code QEB
Advisory panel: Anesthesiology
Date received: 2022-09-23
Decision date: 2023-03-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sao Paulo, BR

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