MolecuLightDX— 510(k) K211901

Substantially Equivalent

MolecuLight, Inc.

FDA 510(k) clearance K211901 for MolecuLightDX, Substantially Equivalent on 2021-07-21. Applicant: MolecuLight, Inc..

Clearance details

Applicant: MolecuLight, Inc.
Product code: Code QJF
Advisory panel: General, Plastic Surgery
Date received: 2021-06-21
Decision date: 2021-07-21
Decision: Substantially Equivalent
Clearance type: Special
Location: Toronto, CA

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