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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