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FDA 510(k) Application Details - K151101
Device Classification Name
Instrument, Ultrasonic Surgical
More FDA Info for this Device
510(K) Number
K151101
Device Name
Instrument, Ultrasonic Surgical
Applicant
SRA DEVELOPMENTS, LTD.
BREMRIDGE HOUSE
ASHBURTON, DEVON TQ13 7JX GB
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Contact
Alan Chivers
Other 510(k) Applications for this Contact
Regulation Number
000.0000
More FDA Info for this Regulation Number
Classification Product Code
LFL
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/24/2015
Decision Date
07/17/2015
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
-
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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