ClearanceBrief
510(k) K192143 ยท NHJ Device, Positive Pressure Breathing, Intermittent

Maximus System

ApplicantHill-Rom Services Pte, Ltd., Singapore, SG
DecisionSubstantially Equivalent, Feb 14, 2020
ReceivedAug 8, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K192143

DateFirm and productCodeLinked 510(k)
Jul 1, 2026Baxter Healthcare Corporation
Hillrom VOLARA System P.CIRCUIT KIT (Single Patient Use Circuit), Model/Catalog Number REF M08085; Oscillation Lung Expansion Therapy, positive pressure breathing device
Open, Classified
NHJNone listed
Jul 1, 2026Baxter Healthcare Corporation
Hillrom VOLARA P.CIRCUIT 5KIT (System Single Patient Use Circuit), Model/Catalog Number REF M08270; Oscillation Lung Expansion Therapy, positive pressure breathing device
Open, Classified
NHJNone listed
Jul 1, 2026Baxter Healthcare Corporation
Hillrom VOLARA System P.CIRCUIT KIT AC (Single Patient Use Circuit), Model/Catalog Number REF M08473; Oscillation Lung Expansion Therapy, positive pressure breathing device
Open, Classified
NHJNone listed
Jul 1, 2026Baxter Healthcare Corporation
Hillrom VOLARA System P.CIRCUIT 5KIT AC, (Single Patient Use Circuit), Model/Catalog Number REF M08474; Oscillation Lung Expansion Therapy, positive pressure breathing device
Open, Classified
NHJNone listed
Apr 1, 2026Baxter Healthcare Corporation
Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937. Accessory to Baxter Volara Respiratory Therapy system.
Open, Classified
NHJNone listed
Jul 17, 2024Baxter Healthcare Corporation
Volara System. Single Patient Use (SPU) Circuit 5kit for Volara and Single Patient Use (SPU) Circuit kit for Volara. Intermittent positive pressure breathing device.
Open, Classified
NHJNone listed
Jul 17, 2024Baxter Healthcare Corporation
Volara System. Blue Ventilator Adapter Module. Intermittent positive pressure breathing device component.
Open, Classified
NHJNone listed

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