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FDA 510(k) Application Details - K984239
Device Classification Name
Electrosurgical, Cutting & Coagulation & Accessories
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510(K) Number
K984239
Device Name
Electrosurgical, Cutting & Coagulation & Accessories
Applicant
AARON MEDICAL INDUSTRIES
7100 30TH AVE. NORTH
ST. PETERSBURG, FL 33710-2902 US
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Contact
J. ROBERT SARON
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Regulation Number
878.4400
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Classification Product Code
GEI
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More FDA Info for this Product Code
Date Received
11/27/1998
Decision Date
02/10/1999
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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