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FDA 510(k) Application Details - K962525
Device Classification Name
Instrument, Ultrasonic Surgical
More FDA Info for this Device
510(K) Number
K962525
Device Name
Instrument, Ultrasonic Surgical
Applicant
MORWEL CORP.
8000 SOUTH KOLB RD.
TUCSON, AZ 85706 US
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Contact
BRENDA HUNT
Other 510(k) Applications for this Contact
Regulation Number
000.0000
More FDA Info for this Regulation Number
Classification Product Code
LFL
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More FDA Info for this Product Code
Date Received
06/27/1996
Decision Date
09/19/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
-
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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