This website uses cookies.
We use cookies to personalize content and ads, to provide social media features and to analyze our
traffic. We also share informatin about your use of our site with our social media, advertising and
analytics partners who may combine it with other information that you’ve provided to them or that
they’ve collected from your use of their services
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.
© Copyright 2023 American Medical Association
$
