ClearanceBrief
510(k) K030652 ยท FIP Subsystem, Water Purification

MEDRO SPD

ApplicantUsfilter/Ionpure, Inc., Lowell MA, US
DecisionSubstantially Equivalent, Sep 3, 2003
ReceivedFeb 28, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030652

DateFirm and productCodeLinked 510(k)
May 6, 2005U.S. Filter/Ionpure, Inc.
MedRo Rx -Reverse Osmosis System All Models All Voltages, All Voltages
Terminated
FIPNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.