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FDA 510(k) Application Details - K092982
Device Classification Name
Curette, Suction, Endometrial (And Accessories)
More FDA Info for this Device
510(K) Number
K092982
Device Name
Curette, Suction, Endometrial (And Accessories)
Applicant
Panpac Medical Corporation
NO. 202, 6F-1.2, SEC.3
TATONG ROAD
SHI-CHIH CITY, TAIPEI HSIEN 22103 TW
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Contact
Yen-Ming Pan
Other 510(k) Applications for this Contact
Regulation Number
884.1175
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Classification Product Code
HHK
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/28/2009
Decision Date
07/26/2010
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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