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FDA 510(k) Application Details - K973737
Device Classification Name
Laparoscope, Gynecologic (And Accessories)
More FDA Info for this Device
510(K) Number
K973737
Device Name
Laparoscope, Gynecologic (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
Other 510(k) Applications for this Contact
Regulation Number
884.1720
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Classification Product Code
HET
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More FDA Info for this Product Code
Date Received
09/30/1997
Decision Date
12/12/1997
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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