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FDA 510(k) Application Details - K120902
Device Classification Name
System, Suction, Lipoplasty
More FDA Info for this Device
510(K) Number
K120902
Device Name
System, Suction, Lipoplasty
Applicant
THE GID GROUP, INC.
4655 KIRKWOOD COURT
BOULDER, CO 80301 US
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Contact
LEWIS WARD
Other 510(k) Applications for this Contact
Regulation Number
878.5040
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Classification Product Code
MUU
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More FDA Info for this Product Code
Date Received
03/26/2012
Decision Date
08/15/2012
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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