FDA 510(k) Application Details - K991852

Device Classification Name	Unit, Phacofragmentation   More FDA Info for this Device
510(K) Number	K991852
Device Name	Unit, Phacofragmentation
Applicant	SURGICAL DESIGN CORP. 1050 CONNECTICUT AVENUE, NW WASHINGTON, DC 20036-5339 US Other 510(k) Applications for this Company
Contact	WAYNE H MATELSKI Other 510(k) Applications for this Contact
Regulation Number	886.4670   More FDA Info for this Regulation Number
Classification Product Code	HQC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/01/1999
Decision Date	07/07/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review