FDA 510(k) Application Details - K962000

Device Classification Name	Lenses, Soft Contact, Daily Wear   More FDA Info for this Device
510(K) Number	K962000
Device Name	Lenses, Soft Contact, Daily Wear
Applicant	FLEXLENS, INC. S. EAST REGULATORY ASSO., INC. 235 NORTH TALBOT COURT ROSWELL, GA 30076-2480 US Other 510(k) Applications for this Company
Contact	WALLY STIRLING Other 510(k) Applications for this Contact
Regulation Number	886.5925   More FDA Info for this Regulation Number
Classification Product Code	LPL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/22/1996
Decision Date	10/01/1996
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