Medical Device Manufacturer · US , Seneca , SC

Philips Medical Systems Dmc GmbH - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 2013

Recent clearances: Radiography 7300 C, Radiography 7000 M, ProxiDiagnost N90 / Precision CRF (706110, 706400)

Total

Cleared

Denied

Philips Medical Systems Dmc GmbH has 18 FDA 510(k) cleared radiology devices. Based in Seneca, US.

Latest FDA clearance: Jun 2024. Active since 2013.

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

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.

Philips Medical Systems Dmc GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Philips Medical Systems Dmc GmbH

18 devices

1-18 of 18

ProxiDiagnost N90 / Precision CRF (706110, 706400)

Philips Radiology Smart Assistant

SkyPlate Detector for Philips Radiography/Fluoroscopy Systems

Philips CombiDiagnost R90

K163210 · JAA

Radiology · 77d

Cleared Dec 22, 2015

Philips Eleva Workspot with SkyFlow

PHILIPS ELEVA WORKSPOT

K140771 · MQB

Radiology · 29d

Cleared Oct 07, 2013

PHILIPS PIXIUM 4343RC

K131483 · MQB

Radiology · 137d

Philips Medical Systems Dmc GmbH - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Philips Medical Systems Dmc GmbH

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