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FDA 510(k) Application Details - K062720
Device Classification Name
Resectoscope
More FDA Info for this Device
510(K) Number
K062720
Device Name
Resectoscope
Applicant
RICHARD WOLF MEDICAL INSTRUMENTS CORP.
353 CORPORATE WOODS PKWY.
VERNON HILLS, IL 60061 US
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Contact
ROBERT L CASARSA
Other 510(k) Applications for this Contact
Regulation Number
876.1500
More FDA Info for this Regulation Number
Classification Product Code
FJL
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/12/2006
Decision Date
03/22/2007
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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