FDA 510(k) Application Details - K033123

Device Classification Name	Ophthalmoscope, Ac-Powered   More FDA Info for this Device
510(K) Number	K033123
Device Name	Ophthalmoscope, Ac-Powered
Applicant	CARL ZEISS MEDITEC INC 5160 HACIENDA DR. DUBLIN, CA 94568 US Other 510(k) Applications for this Company
Contact	R. MICHAEL CROMPTON Other 510(k) Applications for this Contact
Regulation Number	886.1570   More FDA Info for this Regulation Number
Classification Product Code	HLI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/30/2003
Decision Date	04/20/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review