Philips Anesthesia Care is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Philips Anesthesia Care - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Philips Anesthesia Care has 1 FDA 510(k) cleared medical devices. Based in Rodovre, DK.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Philips Anesthesia Care Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Philips Anesthesia Care
1 devices