FDA 510(k) Application Details - K240508

Device Classification Name	Saliva, Artificial   More FDA Info for this Device
510(K) Number	K240508
Device Name	Saliva, Artificial
Applicant	Laclede, Inc. 2103 E. University Dr. Rancho Dominguez, CA 90220 US Other 510(k) Applications for this Company
Contact	Stephen Pellico Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LFD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/21/2024
Decision Date	04/19/2024
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