FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Venus Epileve

K Number: K200786 · Decision Jun 9, 2020
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
11
Review Days
75

Basic Information

Device Name
Venus Epileve
K Number
K200786
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Venus Concept USA Inc.
Date Received
March 26, 2020
Decision Date
June 9, 2020
Product Code
GEX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEX Powered Laser Surgical Instrument

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GEX), ordered by most recent decision date.

View all

Other Clearances by Venus Concept USA Inc.

K Number Device Name
K221011 AI.ME System
K220592 Venus BlissMAX
K213308 Venus BlissMAX
K211461 Family of Venus RF Systems - Venus Freedom
K201164 Venus Viva MD Device
K191065 Venus VivaTM
K191528 Venus Legacy Pro Device
K190743 Venus Bliss
K182094 Family of Venus RF Systems - Heal
K142910 Legacy BX
Search all 11 clearances from Venus Concept USA Inc. →