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FDA 510(k) Applications Submitted by RENAL SOLUTIONS INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K121497
05/21/2012
VENOFER PUMP
RENAL SOLUTIONS INC.
K093964
12/24/2009
VENOFER PUMP
RENAL SOLUTIONS INC.
K070739
03/16/2007
ALLIENT SORBENT HEMODIALYSIS SYSTEM, MODEL# 1500
RENAL SOLUTIONS INC.
K093362
10/28/2009
2008 HEMODIALYSIS SORBENT SYSTEM
RENAL SOLUTIONS INC.
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