FDA 510(k) Application Details - K222064

Device Classification Name	Powered Laser Surgical Instrument   More FDA Info for this Device
510(K) Number	K222064
Device Name	Powered Laser Surgical Instrument
Applicant	Alma Lasers Inc. 485 Half Day Rd Ste 100 Buffalo Grove, IL 60089 US Other 510(k) Applications for this Company
Contact	Jessica Rivera-Montejo Other 510(k) Applications for this Contact
Regulation Number	878.4810   More FDA Info for this Regulation Number
Classification Product Code	GEX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/13/2022
Decision Date	10/12/2022
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