Philips receives FDA 510(k) clearance for Capsule Surveillance solution - Medical Device Network

Retrieved on: 2022-03-16 09:52:23

Tags for this article:

Click the tags to see associated articles and topics

Philips receives FDA 510(k) clearance for Capsule Surveillance solution - Medical Device Network. View article details on hiswai:

Excerpt

The new solution can use streaming data from any connected medical device ... electronic medical records (EMR) and health information technology ...

Article found on: www.medicaldevice-network.com