MolecuLightDX— 510(k) K211901

Substantially Equivalent

MolecuLight, Inc.

FDA 510(k) clearance K211901 for MolecuLightDX, Substantially Equivalent on 2021-07-21. 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: 2021-06-21
Decision date: 2021-07-21
Decision: Substantially Equivalent
Clearance type: Special
Location: Toronto, CA

Download summary PDF View on FDA.gov ↗

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More clearances from MolecuLight, Inc.

K191371 — MolecuLight i:X2019-12-04
DEN180008 — MolecuLight i:X2018-07-31

Data sourced from openFDA. This site is unofficial and independent of the FDA.