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FDA 510(k) Application Details - K101713
Device Classification Name
System, Suction, Lipoplasty
More FDA Info for this Device
510(K) Number
K101713
Device Name
System, Suction, Lipoplasty
Applicant
HUMAN MED AG
WILHELM-HENNEMANN-STR.9
SCHWERIN 19061 DE
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Contact
INGE MATTHIESEN
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
06/18/2010
Decision Date
06/29/2010
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
Y
Expedited Review
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