FDA 510(k) Application Details - K101182

Device Classification Name	Biomicroscope, Slit-Lamp, Ac-Powered   More FDA Info for this Device
510(K) Number	K101182
Device Name	Biomicroscope, Slit-Lamp, Ac-Powered
Applicant	CARL ZEISS MEDITEC AG 5160 HACIENDA DRIVE DUBLIN, CA 94568 US Other 510(k) Applications for this Company
Contact	JUDITH A BRIMACOMBE Other 510(k) Applications for this Contact
Regulation Number	886.1850   More FDA Info for this Regulation Number
Classification Product Code	HJO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/27/2010
Decision Date	11/03/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review