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FDA 510(k) Application Details - K180819
Device Classification Name
Lenses, Soft Contact, Daily Wear
More FDA Info for this Device
510(K) Number
K180819
Device Name
Lenses, Soft Contact, Daily Wear
Applicant
Menicon Co., Ltd.
21-19, Aoi 3, Naka-ku
Nagoya 460-0006 JP
Other 510(k) Applications for this Company
Contact
Kenichi Tanaka
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
03/29/2018
Decision Date
05/16/2018
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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