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FDA 510(k) Application Details - K030349
Device Classification Name
Analyzer, Body Composition
More FDA Info for this Device
510(K) Number
K030349
Device Name
Analyzer, Body Composition
Applicant
BONSO ELECTRONICS INTERNATIONAL INC.
719 A STREET, NE
WASHINGTON, DC 20002 US
Other 510(k) Applications for this Company
Contact
RUSS PAGANO
Other 510(k) Applications for this Contact
Regulation Number
870.2770
More FDA Info for this Regulation Number
Classification Product Code
MNW
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/03/2003
Decision Date
05/02/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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