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Clinical note: Devices listed for use at home are validated for the population tested and may not always provide accurate BP measurements for a specific individual. Whenever practical, patients are encouraged to bring their home BP devices to the physician's office or other qualified health care

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The Independent Review Committee, comprised of physician experts, assesses if a BP device satisfies the VDL Criteria for validation of clinical accuracy. Devices that meet the Criteria are then published on the listing page. Devices are regularly reviewed and added through this independent process.

Blood pressure measurement devices that have been validated for clinical accuracy as determined through an independent review process.

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The VDL does list devices that measure other biometrics. It is important to note that for those devices, only the BP measurement components have been reviewed for validation of clinical accuracy.

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The American Medical Association (“AMA”) does not receive funding from any third-party in relation to the development of the Validated Device Listing Criteria (“VDL™ Criteria”), and does not receive funding from any blood pressure (“BP”) device manufacturer or other third-party in relation to the development of the VDL process. No recommendation, promotion, or endorsement is implied or intended by the AMA (or any of the AMA's affiliated or partner organizations) of any third-party organization, product, device, policy, or service. BP measurement devices are selected to appear on the VDL through an independent review process that determines which available BP measurement devices meet established VDL Criteria for the validation of clinical accuracy. An Independent Review Committee, composed of members who are experts in the BP field, assess whether a BP measurement device satisfies the VDL Criteria. The ultimate judgment regarding whether a BP measurement device meets the requisite VDL Criteria rests with the Independent Review Committee, and is not in any way determined or influenced by the AMA.

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The AMA does not receive funding from any device manufacturer or other third party in relation to the development of the VDL Criteria or VDL process.*

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The ultimate judgment regarding whether a BP measurement device meets the requisite VDL Criteria rests with the Independent Review Committee and is not in any way determined or influenced by the AMA.