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FDA 510(k) Application Details - K070023
Device Classification Name
System, Ablation, Microwave And Accessories
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510(K) Number
K070023
Device Name
System, Ablation, Microwave And Accessories
Applicant
MICROSURGEON, INC.
20662 EAST TULIP CIRCLE
MONTROSE, CO 81401 US
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Contact
DUDLEY HARRIS
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Regulation Number
878.4400
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Classification Product Code
NEY
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More FDA Info for this Product Code
Date Received
01/03/2007
Decision Date
08/15/2007
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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