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FDA 510(k) Applications Submitted by RENAL SOLUTIONS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K103564
12/06/2010
VENOFER PUMP
RENAL SOLUTIONS, INC.
K123835
12/13/2012
2008 HEMODIALYSIS SORBENT SYSTEM
RENAL SOLUTIONS, INC.
K060381
02/14/2006
ALLIENT SORBET HEMODIALYSIS SYSTEM, MODEL 1100
RENAL SOLUTIONS, INC.
K043574
12/27/2004
ALLIENT SORBENT HEMODIALYSIS SYSTEM, MODEL 1000
RENAL SOLUTIONS, INC.
K031099
04/07/2003
SORB+HISORB+CARTRIDGE
RENAL SOLUTIONS, INC.
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