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FDA 510(k) Application Details - K032772
Device Classification Name
System, Monitoring, Perinatal
More FDA Info for this Device
510(K) Number
K032772
Device Name
System, Monitoring, Perinatal
Applicant
HILL-ROM MANUFACTURING, INC.
1225 CRESCENT GREEN
SUITE 200
CARY, NC 27511 US
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Contact
CINDY L CROSBY
Other 510(k) Applications for this Contact
Regulation Number
884.2740
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Classification Product Code
HGM
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
09/08/2003
Decision Date
10/08/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OB - Obstetrics/Gynecology
Review Advisory Committee
OB - Obstetrics/Gynecology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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