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FDA 510(k) Application Details - K024059
Device Classification Name
Electrosurgical, Cutting & Coagulation & Accessories
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510(K) Number
K024059
Device Name
Electrosurgical, Cutting & Coagulation & Accessories
Applicant
SORING GMBH MEDIZINTECHNIK
1100 LAKEVIEW BLVD.
DENTON, TX 76208 US
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Contact
CARL ALLETTO
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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
12/09/2002
Decision Date
01/08/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
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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