FDA 510(k) Application Details - K233435

Device Classification Name	Masker, Tinnitus   More FDA Info for this Device
510(K) Number	K233435
Device Name	Masker, Tinnitus
Applicant	PNQ Health 110 Cheshire Lane Ste 385 Minnetonka, MN 55305 US Other 510(k) Applications for this Company
Contact	Kurtis Goos Other 510(k) Applications for this Contact
Regulation Number	874.3400   More FDA Info for this Regulation Number
Classification Product Code	KLW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/13/2023
Decision Date	02/27/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	EN - Ear, Nose, & Throat
Review Advisory Committee	EN - Ear, Nose, & Throat
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review