ClearanceBrief
510(k) K223843 ยท DPW Flowmeter, Blood, Cardiovascular

FloPatch FP120

ApplicantFlosonics Medical, Toronto, CA
DecisionSubstantially Equivalent, May 3, 2023
ReceivedDec 22, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K223843

DateFirm and productCodeLinked 510(k)
Sep 4, 2025Flosonics Medical (R/A 1929803 ONTARIO CORP.)
FloPatch FP120, REF: FP120-FOT01-005
Open, Classified
DPWNone listed

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