FDA 510(k) Application Details - K172208

Device Classification Name	Tube, Tracheal (W/Wo Connector)   More FDA Info for this Device
510(K) Number	K172208
Device Name	Tube, Tracheal (W/Wo Connector)
Applicant	NeVap, Inc. 975 Dionne Way San Jose, CA 95133 US Other 510(k) Applications for this Company
Contact	Brenton Hanlon Other 510(k) Applications for this Contact
Regulation Number	868.5730   More FDA Info for this Regulation Number
Classification Product Code	BTR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/24/2017
Decision Date	02/16/2018
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