FDA 510(k) Application Details - K954943

Device Classification Name	Device, Medical Examination, Ac Powered   More FDA Info for this Device
510(K) Number	K954943
Device Name	Device, Medical Examination, Ac Powered
Applicant	NIZAR A. MULLANI 719 SANTA MARIA SUGARLAND, TX 77478 US Other 510(k) Applications for this Company
Contact	NIZAR A MULLANI Other 510(k) Applications for this Contact
Regulation Number	880.6320   More FDA Info for this Regulation Number
Classification Product Code	KZF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/30/1995
Decision Date	03/27/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review