Question Category: Submission & Device Selection

Who determines which devices are included on the list?

What does the submission process consist of?

Does this list mean the AMA endorses any of these devices?

How trustworthy is this list now?

How does the AMA process differ from the FDA process to approve blood pressure devices?

What types of BP devices made the VDL?

I recently bought a BP device that isn’t on the list. Will it be added?

How often are devices added to the list?