Enlight 1810— 510(k) DEN170072

Unknown

Timpel, Inc.

FDA 510(k) clearance DEN170072 for Enlight 1810, Unknown on 2018-12-20. Applicant: Timpel, Inc.. Device class: 2.

Clearance details

Applicant: Timpel, Inc.
Product code: Code QEB
Device class: Class 2
Regulation: 21 CFR 868.1505
Advisory panel: Anesthesiology
Date received: 2017-09-29
Decision date: 2018-12-20
Decision: Unknown
Clearance type: Direct
Location: Sao Paulo-Sp, BR

View on FDA.gov ↗

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