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FDA 510(k) Application Details - K062471
Device Classification Name
Instrument, Ultrasonic Surgical
More FDA Info for this Device
510(K) Number
K062471
Device Name
Instrument, Ultrasonic Surgical
Applicant
MISONIX, INC.
1938 NEW HIGHWAY
FARMINGDALE, NY 11735 US
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Contact
RONALD R MANNA
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
08/24/2006
Decision Date
10/26/2006
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
-
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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