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FDA 510(k) Application Details - K173332
Device Classification Name
Pump, Infusion, Ophthalmic
More FDA Info for this Device
510(K) Number
K173332
Device Name
Pump, Infusion, Ophthalmic
Applicant
Sight Sciences, Inc.
3000 Sand Hill Road
Building 3, Suite 105
Menlo Park, CA 94025 US
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Contact
Anne-Marie Ripley
Other 510(k) Applications for this Contact
Regulation Number
880.5725
More FDA Info for this Regulation Number
Classification Product Code
MRH
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More FDA Info for this Product Code
Date Received
10/23/2017
Decision Date
12/21/2017
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
OP - Ophthalmic
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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