FDA 510(k) Application Details - K021634

Device Classification Name	Airway, Oropharyngeal, Anesthesiology   More FDA Info for this Device
510(K) Number	K021634
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	05/17/2002
Decision Date	01/09/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review