FDA 510(k) Application Details - K022373

Device Classification Name	Lens, Spectacle (Prescription), For Reading Discomfort   More FDA Info for this Device
510(K) Number	K022373
Device Name	Lens, Spectacle (Prescription), For Reading Discomfort
Applicant	CANTOR & NISSEL LTD. 623 GLACIER DR. GRAND JUCTION, CO 81503 US Other 510(k) Applications for this Company
Contact	MARTIN DALSING Other 510(k) Applications for this Contact
Regulation Number	886.5844   More FDA Info for this Regulation Number
Classification Product Code	NJH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/22/2002
Decision Date	10/07/2002
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