FDA 510(k) Application Details - K082767

Device Classification Name	Camera, Ophthalmic, Ac-Powered   More FDA Info for this Device
510(K) Number	K082767
Device Name	Camera, Ophthalmic, Ac-Powered
Applicant	KOWA CO. LTD. 4-14, NIHONBASHI-HONCHO 3-CHOME CHUO-KU, TOKYO 103-8433 JP Other 510(k) Applications for this Company
Contact	AKIHIRO FUJITA Other 510(k) Applications for this Contact
Regulation Number	886.1120   More FDA Info for this Regulation Number
Classification Product Code	HKI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/22/2008
Decision Date	10/21/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review