Phillips Medical Systems is one of 491 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Phillips Medical Systems - FDA 510(k) Cleared Devices
Recent clearances: SureSigns VS3, SureSigns VS4, INTELLIVUE MX40 PATIENT MONITOR, HD7 DIAGNOSTIC ULTRASOUND SYSTEM
4
Total
4
Cleared
0
Denied
Phillips Medical Systems has 4 FDA 510(k) cleared medical devices. Based in Boblingen, DE.
Historical record: 4 cleared submissions from 2004 to 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Phillips Medical Systems Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Phillips Medical Systems
4 devices