FDA 510(k) Application Details - K022186

Device Classification Name	Plug, Scleral   More FDA Info for this Device
510(K) Number	K022186
Device Name	Plug, Scleral
Applicant	MICROVISION, INC. 34 FOLLY MILL RD. SUITE 200 P.O. BOX 1651 SEABROOK, NH 03874-1651 US Other 510(k) Applications for this Company
Contact	LEONARD KASTRILEVICH Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LXP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/05/2002
Decision Date	02/26/2003
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