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FDA 510(k) Application Details - K050583
Device Classification Name
System, Monitoring, Perinatal
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510(K) Number
K050583
Device Name
System, Monitoring, Perinatal
Applicant
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
4502 WOODLAND CORPORATE BLVD.
TAMPA, FL 33614 US
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Contact
MELISSA ROBINSON
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Regulation Number
884.2740
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Classification Product Code
HGM
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More FDA Info for this Product Code
Date Received
03/07/2005
Decision Date
06/21/2005
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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