FDA 510(k) Application Details - K945301

Device Classification Name	Laryngoscope, Rigid   More FDA Info for this Device
510(K) Number	K945301
Device Name	Laryngoscope, Rigid
Applicant	SOTIRIA MOURKIDOU, M.D. 27112 MALIBU COVE COLONY DR. MALIBU, CA 90265 US Other 510(k) Applications for this Company
Contact	SOTIRIA MOURKIDOU 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	10/31/1994
Decision Date	05/31/1996
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