Venus BlissMAX— 510(k) K220592

Substantially Equivalent

Venus Concept USA, Inc.

FDA 510(k) clearance K220592 for Venus BlissMAX, Substantially Equivalent on 2022-04-27. Applicant: Venus Concept USA, Inc.. Device class: 2.

Clearance details

Applicant: Venus Concept USA, Inc.
Product code: Code PBX
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 2022-03-01
Decision date: 2022-04-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Weston, FL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Venus Concept USA, Inc.

K221011 — AI.ME System2022-12-20
K213308 — Venus BlissMAX2022-01-12
K211461 — Family of Venus RF Systems - Venus Freedom2021-10-14
K201164 — Venus Viva MD Device2020-06-26
K200786 — Venus Epileve2020-06-09

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