Lumenis Stellar M22— 510(k) DEN200028
UnknownLumenis, Ltd.
FDA 510(k) clearance DEN200028 for Lumenis Stellar M22, Unknown on 2021-02-23. Applicant: Lumenis, Ltd.. Device class: 2.
Clearance details
- Applicant
- Lumenis, Ltd.
- Product code
- Code QIU
- Device class
- Class 2
- Regulation
- 21 CFR 886.5201
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Yokneam, IL
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Data sourced from openFDA. This site is unofficial and independent of the FDA.