FDA 510(k) Application Details - K992950

Device Classification Name	Lenses, Soft Contact, Daily Wear   More FDA Info for this Device
510(K) Number	K992950
Device Name	Lenses, Soft Contact, Daily Wear
Applicant	PROSTHETIC SOFT LENS CORP. 2890 SOUTH TEJON ST. ENGLEWOOD, CO 80110 US Other 510(k) Applications for this Company
Contact	WILLIAM HOFFMAN 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	09/01/1999
Decision Date	11/18/1999
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