FDA 510(k) Application Details - K172994

Device Classification Name	Keratome, Ac-Powered   More FDA Info for this Device
510(K) Number	K172994
Device Name	Keratome, Ac-Powered
Applicant	Moria SA 15 Rue Georges Besse Antony FR Other 510(k) Applications for this Company
Contact	Jean-Paul Mercereau Other 510(k) Applications for this Contact
Regulation Number	886.4370   More FDA Info for this Regulation Number
Classification Product Code	HNO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/27/2017
Decision Date	10/26/2017
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