FDA 510(k) Application Details - K062231

Device Classification Name	Laryngoscope, Rigid   More FDA Info for this Device
510(K) Number	K062231
Device Name	Laryngoscope, Rigid
Applicant	MINRAD, INC. 847 MAIN ST. BUFFALO, NY 14203 US Other 510(k) Applications for this Company
Contact	JOHN MCNEIRNEY Other 510(k) Applications for this Contact
Regulation Number	868.5540   More FDA Info for this Regulation Number
Classification Product Code	CCW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/02/2006
Decision Date	08/31/2006
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