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FDA 510(k) Application Details - K000376
Device Classification Name
Lenses, Soft Contact, Daily Wear
More FDA Info for this Device
510(K) Number
K000376
Device Name
Lenses, Soft Contact, Daily Wear
Applicant
SPECIALTY ULTRAVISION, INC.
307 ORCHARD CITY DR.
CAMPBELL, CA 95008 US
Other 510(k) Applications for this Company
Contact
GAROLD L EDWARDS
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
02/07/2000
Decision Date
03/21/2000
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
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