Medical Device Manufacturer · US , Andover , MA

Philips Medizin Systeme Boblingen GmbH - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 2001

Recent clearances: Philips IntelliVue GuardianSoftware, PHILIPS AVALON FETAL / MATERNAL MONITORS FM20, FM30, FM40 AND FM50, INTELLIVUE PATIENT MONITOR

12
Total
12
Cleared
0
Denied

Philips Medizin Systeme Boblingen GmbH has 12 FDA 510(k) cleared cardiovascular devices. Based in Andover, US.

Historical record: 12 cleared submissions from 2001 to 2015.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Philips Medizin Systeme Boblingen GmbH

12 devices
1-12 of 12
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