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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