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FDA 510(k) Application Details - K974735
Device Classification Name
Electrode, Electrosurgical
More FDA Info for this Device
510(K) Number
K974735
Device Name
Electrode, Electrosurgical
Applicant
AARON MEDICAL INDUSTRIES
7100 30TH AVE. NORTH
ST. PETERSBURG, FL 33710-2902 US
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Contact
J. ROBERT SARON
Other 510(k) Applications for this Contact
Regulation Number
878.4400
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Classification Product Code
JOS
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More FDA Info for this Product Code
Date Received
12/18/1997
Decision Date
06/24/1998
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
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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