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FDA 510(k) Application Details - K162932
Device Classification Name
System, Suction, Lipoplasty
More FDA Info for this Device
510(K) Number
K162932
Device Name
System, Suction, Lipoplasty
Applicant
RANFAC CORP.
30 DOHERTY AVENUE,
P.O. BOX 635
Avon, MA 02322 US
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Contact
CHRISTOPHER WHELAN
Other 510(k) Applications for this Contact
Regulation Number
878.5040
More FDA Info for this Regulation Number
Classification Product Code
MUU
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
10/20/2016
Decision Date
01/19/2017
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
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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