FDA 510(k) Application Details - K945590

Device Classification Name	Laryngoscope, Rigid   More FDA Info for this Device
510(K) Number	K945590
Device Name	Laryngoscope, Rigid
Applicant	SMITH HELMS MULLISS & MOORE, L.L.P. POST OFFICE BOX 21927 GREENSBORO, NC 27420 US Other 510(k) Applications for this Company
Contact	CHRISTINE T NERO 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	11/14/1994
Decision Date	05/20/1997
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