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FDA 510(k) Application Details - K211104
Device Classification Name
Insufflator, Laparoscopic
More FDA Info for this Device
510(K) Number
K211104
Device Name
Insufflator, Laparoscopic
Applicant
ConMed Corporation
525 French Road
Utica, NY 13502 US
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Contact
Ally Xu
Other 510(k) Applications for this Contact
Regulation Number
884.1730
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Classification Product Code
HIF
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More FDA Info for this Product Code
Date Received
04/13/2021
Decision Date
08/19/2021
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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