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FDA 510(k) Application Details - K020930
Device Classification Name
Products, Contact Lens Care, Rigid Gas Permeable
More FDA Info for this Device
510(K) Number
K020930
Device Name
Products, Contact Lens Care, Rigid Gas Permeable
Applicant
MENICON CO. LTD.
269A BALLARDVALE ST.
WILMINGTON, MA 01887 US
Other 510(k) Applications for this Company
Contact
BEVERLEY D VENUTI
Other 510(k) Applications for this Contact
Regulation Number
886.5918
More FDA Info for this Regulation Number
Classification Product Code
MRC
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/22/2002
Decision Date
05/02/2002
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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