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FDA 510(k) Application Details - K022503
Device Classification Name
Cannula, Manipulator/Injector, Uterine
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510(K) Number
K022503
Device Name
Cannula, Manipulator/Injector, Uterine
Applicant
THOMAS MEDICAL, INC.
4100-C NINE MCFARLAND DR.
ALPHARETTA, GA 30004 US
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Contact
THOMAS J ZINNANTI
Other 510(k) Applications for this Contact
Regulation Number
000.0000
More FDA Info for this Regulation Number
Classification Product Code
LKF
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
07/29/2002
Decision Date
10/25/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OB - Obstetrics/Gynecology
Review Advisory Committee
OB - Obstetrics/Gynecology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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