FDA 510(k) Application Details - K241600

Device Classification Name	Powered Laser Surgical Instrument   More FDA Info for this Device
510(K) Number	K241600
Device Name	Powered Laser Surgical Instrument
Applicant	Asclepion Laser Technologies GmbH Bruesseler Strasse 10 Jena 07745 DE Other 510(k) Applications for this Company
Contact	Tom Gruender 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	06/04/2024
Decision Date	07/03/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review