MolecuLight I:X— 510(k) K213840
Substantially EquivalentMolecuLight, Inc.
FDA 510(k) clearance K213840 for MolecuLight I:X, Substantially Equivalent on 2022-05-18. Applicant: MolecuLight, Inc.. Device class: 2.
Clearance details
- Applicant
- MolecuLight, Inc.
- Product code
- Code QJF
- Device class
- Class 2
- Regulation
- 21 CFR 878.4550
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Toronto, CA
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