FDA 510(k) Application Details - K082420

Device Classification Name	Tube, Tracheal (W/Wo Connector)   More FDA Info for this Device
510(K) Number	K082420
Device Name	Tube, Tracheal (W/Wo Connector)
Applicant	ETVIEW 31 HAAVODA ST BINYAMINA 30500 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	08/22/2008
Decision Date	10/08/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review