FDA 510(k) Application Details - K223681

Device Classification Name	Monitor, Breathing Frequency   More FDA Info for this Device
510(K) Number	K223681
Device Name	Monitor, Breathing Frequency
Applicant	Respiree PTE Ltd. 115 East Coast Rd Singapore 428804 SG Other 510(k) Applications for this Company
Contact	Gurpreet Singh Other 510(k) Applications for this Contact
Regulation Number	868.2375   More FDA Info for this Regulation Number
Classification Product Code	BZQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/08/2022
Decision Date	03/08/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review