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FDA 510(k) Application Details - K172066
Device Classification Name
Lenses, Soft Contact, Daily Wear
More FDA Info for this Device
510(K) Number
K172066
Device Name
Lenses, Soft Contact, Daily Wear
Applicant
Alcon Laboratories, Inc.
6201 South Freeway
Fort Worth, TX 76134-2099 US
Other 510(k) Applications for this Company
Contact
Sherri Lakota
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
07/07/2017
Decision Date
08/09/2017
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OP - Ophthalmic
Review Advisory Committee
OP - Ophthalmic
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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