Philips Medical Systems Dmc GmbH
Philips Medical Systems Dmc GmbH holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2024, with 11 FDA device recalls on record.
Top product codes for Philips Medical Systems Dmc GmbH
FDA recalls by Philips Medical Systems Dmc GmbH
10 most recent of 11- Z-0466-2026 — Radiography 7300 C; Model Number: 712037;
- Z-0462-2026 — CombiDiagnost R90; Model Number: 709031;
- Z-0464-2026 — DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 712031, (2) 712032;
- Z-0463-2026 — Precision CRF; Model Number: 706400;
- Z-0461-2026 — ProxiDiagnost N90; Model Number: 706110;
- Z-0465-2026 — DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035;
- Z-1327-2022 — DigitalDiagnost 4 Flex / Value. radiography and fluoroscopy system
- Z-1325-2022 — ProxiDiagnost N90. radiography and fluoroscopy system
- Z-1326-2022 — DigitalDiagnost 4 High Performance. radiography and fluoroscopy system
- Z-1328-2022 — DigitalDiagnost C90 High Performance. radiography and fluoroscopy system
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Philips Medical Systems Dmc GmbH
- K233662 — Radiography 7300 C
- K233678 — Radiography 7000 M
- K233945 — ProxiDiagnost N90 / Precision CRF (706110, 706400)
- K232910 — CombiDiagnost R90
- K212186 — Philips Radiology Smart Assistant
- K212837 — ProxiDiagnost N90
- K210692 — DigitalDiagnost
- K203087 — CombiDiagnost R90
- K202564 — DigitalDiagnost C90
- K182973 — DigitalDiagnost C90
- K173433 — ProxiDiagnost N90
- K171461 — SkyPlate Detector for Philips Radiography/Fluoroscopy Systems
- K170113 — pixium 4343RCE
- K163210 — Philips CombiDiagnost R90
- K153318 — Philips Eleva Workspot with SkyFlow
- K141736 — PHILIPS PROGRADE; PHILIPS ELEVA WORKSPOT FOR DIGITAL DIAGNOST
- K140771 — PHILIPS ELEVA WORKSPOT
- K131483 — PHILIPS PIXIUM 4343RC
Data sourced from openFDA. This site is unofficial and independent of the FDA.