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FDA 510(k) Application Details - K002835
Device Classification Name
Analyzer, Body Composition
More FDA Info for this Device
510(K) Number
K002835
Device Name
Analyzer, Body Composition
Applicant
BODYSTAT LTD.
PO BOX 50
DOUGLAS ISLE OF MAN
BRITISH ISLES IM99 1DQ GB
Other 510(k) Applications for this Company
Contact
I.J. MEEUWSEN
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
09/12/2000
Decision Date
07/03/2001
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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