Lumenis Stellar M22— 510(k) DEN200028

Unknown

Lumenis, Ltd.

FDA 510(k) clearance DEN200028 for Lumenis Stellar M22, Unknown on 2021-02-23. Applicant: Lumenis, Ltd..

Clearance details

Applicant: Lumenis, Ltd.
Product code: Code QIU
Advisory panel: Ophthalmic
Date received: 2020-04-20
Decision date: 2021-02-23
Decision: Unknown
Clearance type: Direct
Location: Yokneam, IL

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