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FDA 510(k) Application Details - K955900
Device Classification Name
Lens, Contact (Other Material) - Daily
More FDA Info for this Device
510(K) Number
K955900
Device Name
Lens, Contact (Other Material) - Daily
Applicant
NOVAVISION, INC.
2700-200 GATEWAY CENTRE BLVD.
MORRISVILLE, NC 27560 US
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Contact
ALAN J TOUCH
Other 510(k) Applications for this Contact
Regulation Number
886.5916
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Classification Product Code
HQD
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More FDA Info for this Product Code
Date Received
12/29/1995
Decision Date
03/25/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OP - Ophthalmic
Review Advisory Committee
OP - Ophthalmic
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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