FDA 510(k) Application Details - K052233

Device Classification Name	Tube, Tracheal (W/Wo Connector)   More FDA Info for this Device
510(K) Number	K052233
Device Name	Tube, Tracheal (W/Wo Connector)
Applicant	ETVIEW LTD. 31 HAAVODA ST. BINYAMINA IL Other 510(k) Applications for this Company
Contact	YORAM LEVY 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	08/17/2005
Decision Date	12/13/2005
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