FDA 510(k) Application Details - K091915

Device Classification Name	Unit, Phacofragmentation   More FDA Info for this Device
510(K) Number	K091915
Device Name	Unit, Phacofragmentation
Applicant	LENSTEC, INC. 1765 COMMERCE AVE N ST. PETERSBURG, FL 33716 US Other 510(k) Applications for this Company
Contact	JIMMY CHACKO 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	06/30/2009
Decision Date	10/27/2009
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