FDA 510(k) Application Details - K033189

Device Classification Name	Airway, Oropharyngeal, Anesthesiology   More FDA Info for this Device
510(K) Number	K033189
Device Name	Airway, Oropharyngeal, Anesthesiology
Applicant	KING SYSTEMS CORP. 15011 HERRIMAN BLVD. NOBLESVILLE, IN 46060 US Other 510(k) Applications for this Company
Contact	TOM MCGRAIL Other 510(k) Applications for this Contact
Regulation Number	868.5110   More FDA Info for this Regulation Number
Classification Product Code	CAE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/01/2003
Decision Date	05/04/2004
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