Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K230720
Device Classification Name
Over-The-Counter Powered Light Based Laser For Acne
More FDA Info for this Device
510(K) Number
K230720
Device Name
Over-The-Counter Powered Light Based Laser For Acne
Applicant
Light Tree Ventures Europe B.V.
Laan van Ypenburg 108, 2497 GC, The Hague, The Netherlands
Hague NL
Other 510(k) Applications for this Company
Contact
Kim Laurens
Other 510(k) Applications for this Contact
Regulation Number
878.4810
More FDA Info for this Regulation Number
Classification Product Code
OLP
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/16/2023
Decision Date
07/03/2023
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact