MolecuLight i:X— 510(k) DEN180008
UnknownMolecuLight, Inc.
FDA 510(k) clearance DEN180008 for MolecuLight i:X, Unknown on 2018-07-31. Applicant: MolecuLight, Inc.. Device class: 1.
Clearance details
- Applicant
- MolecuLight, Inc.
- Product code
- Code QCR
- Device class
- Class 1
- Regulation
- 21 CFR 878.4165
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Toronto, CA
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