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FDA 510(k) Application Details - K962121
Device Classification Name
Lenses, Soft Contact, Daily Wear
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510(K) Number
K962121
Device Name
Lenses, Soft Contact, Daily Wear
Applicant
WESTCON CONTACT LENS CO., INC.
611 EISENHAUER ST.
GRAND JUNCTION, CO 81505 US
Other 510(k) Applications for this Company
Contact
MARTIN DALSING
Other 510(k) Applications for this Contact
Regulation Number
886.5925
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Classification Product Code
LPL
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
05/31/1996
Decision Date
08/26/1996
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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