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FDA 510(k) Application Details - K172844
Device Classification Name
More FDA Info for this Device
510(K) Number
K172844
Device Name
Cellvizio 100 Series System with Confocal Miniprobes
Applicant
Mauna Kea Technologies
9 Rue d'Enghien
Paris 75010 FR
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Contact
Veronique Dentan
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Regulation Number
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Classification Product Code
OWN
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More FDA Info for this Product Code
Date Received
09/19/2017
Decision Date
12/15/2017
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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