ClearanceBrief
510(k) K072105 ยท FRN Pump, Infusion

ALARIS SYSTEM WITH MMS, MODEL 8XXX

ApplicantCardinal Health 303,Inc., San Diego CA, US
DecisionSubstantially Equivalent, Dec 28, 2007
ReceivedJul 31, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K072105

DateFirm and productCodeLinked 510(k)
Mar 26, 2026CareFusion 303, Inc.
BD Alaris" System with Guardrails" Suite MX with Point of Care Unit
Open, Classified
FRNNone listed
Nov 7, 2023CareFusion 303, Inc.
BD Alaris PCU REF 8015
Open, Classified
FRNNone listed
Nov 7, 2023CareFusion 303, Inc.
BD Alaris Syringe Module, REF 8110
Open, Classified
FRNNone listed
Nov 7, 2023CareFusion 303, Inc.
Alaris PCA Module 8120
Open, Classified
FRNNone listed
Mar 1, 2023CareFusion 303, Inc.
Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses from x.x.x.224 to x.x.x.255
Open, Classified
FRNNone listed

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