FDA 510(k) Application Details - K121405

Device Classification Name	Camera, Ophthalmic, Ac-Powered   More FDA Info for this Device
510(K) Number	K121405
Device Name	Camera, Ophthalmic, Ac-Powered
Applicant	WELCH ALLYN, INC. 4341 STATE ST. RD. PO BOX 220 SKANEATELES FALLS, NY 13153-0020 US Other 510(k) Applications for this Company
Contact	KEVIN CROSSEN 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	05/10/2012
Decision Date	12/20/2012
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