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FDA 510(k) Applications Submitted by U.S. FILTER/IONPURE, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K980182
01/20/1998
WATER PURIFICATION SYSTEM FOR HEMODIALYSIS
U.S. FILTER/IONPURE, INC.
K013677
11/07/2001
MODIFICATION TO: MED-RO REVERSE OSMOSIS SYSTEM
U.S. FILTER/IONPURE, INC.
K030652
02/28/2003
MEDRO SPD
U.S. FILTER/IONPURE, INC.
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