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FDA 510(k) Application Details - K991895
Device Classification Name
Curette, Suction, Endometrial (And Accessories)
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510(K) Number
K991895
Device Name
Curette, Suction, Endometrial (And Accessories)
Applicant
RI MOS. S.R.L.
100 MAIN ST.
SUITE 120
CONCORD, MA 01742 US
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Contact
JAMES DELANEY
Other 510(k) Applications for this Contact
Regulation Number
884.1175
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Classification Product Code
HHK
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More FDA Info for this Product Code
Date Received
06/03/1999
Decision Date
08/12/1999
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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