FDA 510(k) Application Details - K062930

Device Classification Name	Aberrometer, Ophthalmic   More FDA Info for this Device
510(K) Number	K062930
Device Name	Aberrometer, Ophthalmic
Applicant	ALCON RESEARCH, LTD. 2501 DISCOVERY DR. SUITE 500 ORLANDO, FL 32826 US Other 510(k) Applications for this Company
Contact	JANET G JOHNSON Other 510(k) Applications for this Contact
Regulation Number	886.1760   More FDA Info for this Regulation Number
Classification Product Code	NCF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/28/2006
Decision Date	11/08/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review