TFX-LT2000 Therapy Light— 510(k) K211265

Substantially Equivalent

Toefx, Inc.

FDA 510(k) clearance K211265 for TFX-LT2000 Therapy Light, Substantially Equivalent on 2022-11-17. Applicant: Toefx, Inc.. Device class: 2.

Clearance details

Applicant: Toefx, Inc.
Product code: Code PDZ
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2021-04-26
Decision date: 2022-11-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hamilton, CA

Download summary PDF View on FDA.gov ↗

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