FDA 510(k) Application Details - K232025

Device Classification Name	Device, Anti-Snoring   More FDA Info for this Device
510(K) Number	K232025
Device Name	Device, Anti-Snoring
Applicant	Good Sleep Co Pte Ltd. 226 Ocean Drive Singapore 098617 SG Other 510(k) Applications for this Company
Contact	Joel Simoson Other 510(k) Applications for this Contact
Regulation Number	872.5570   More FDA Info for this Regulation Number
Classification Product Code	LRK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/07/2023
Decision Date	05/09/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review