ClearanceBrief
510(k) K241411 · MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

Welch Allyn Connex® Spot Monitor; 901058 Vital Signs Monitor Core (CSM)

ApplicantWelch Allyn, Inc., Skaneateles Falls NY, US
DecisionSubstantially Equivalent, Dec 20, 2024
ReceivedMay 17, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K241411

DateFirm and productCodeLinked 510(k)
Apr 14, 2025Baxter Healthcare Corporation
Welch Allyn CONNEX Accessory Power Management Stand:
Open, Classified
MWINone listed

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