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FDA 510(k) Application Details - K990147
Device Classification Name
Coagulator-Cutter, Endoscopic, Bipolar (And Accessories)
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510(K) Number
K990147
Device Name
Coagulator-Cutter, Endoscopic, Bipolar (And Accessories)
Applicant
RICHARD WOLF MEDICAL INSTRUMENTS CORP.
353 CORPORATE WOODS PKWY.
VERNON HILLS, IL 60061 US
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Contact
ROBERT L CASARSA
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Regulation Number
884.4150
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Classification Product Code
HIN
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More FDA Info for this Product Code
Date Received
01/19/1999
Decision Date
04/16/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OB - Obstetrics/Gynecology
Review Advisory Committee
OB - Obstetrics/Gynecology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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