FDA 510(k) Application Details - K981742

Device Classification Name	Keratome, Ac-Powered   More FDA Info for this Device
510(K) Number	K981742
Device Name	Keratome, Ac-Powered
Applicant	MORIA, INC. 15 RUE GEORGES BESSE ANTONY 92160 FR Other 510(k) Applications for this Company
Contact	ALAIN DUPRAT 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	05/18/1998
Decision Date	08/25/1998
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