FDA 510(k) Application Details - K241354

Device Classification Name	Cleanser, Root Canal   More FDA Info for this Device
510(K) Number	K241354
Device Name	Cleanser, Root Canal
Applicant	Inter-Med, Inc. 2200 South Street Racine, WI 53575 US Other 510(k) Applications for this Company
Contact	Brett Arand Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	KJJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/13/2024
Decision Date	08/27/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review