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FDA 510(k) Application Details - K060296
Device Classification Name
Subsystem, Proportioning
More FDA Info for this Device
510(K) Number
K060296
Device Name
Subsystem, Proportioning
Applicant
NXSTAGE MEDICAL, INC.
439 SOUTH UNION ST.
SUITE 501
LAWRENCE, MA 01843 US
Other 510(k) Applications for this Company
Contact
NORMA LEMAY
Other 510(k) Applications for this Contact
Regulation Number
876.5820
More FDA Info for this Regulation Number
Classification Product Code
FKR
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/06/2006
Decision Date
03/31/2006
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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