Atlas FDA

Philips Medical Systems DMC GmbH

11 FDA 510(k) clearances · Recalling firm

Sort:Newest firstOldest first

◉ Watch Philips Medical Systems DMC GmbH

RecordFirmDate
ProxiDiagnost N90; Model Number: 706110; recall (Z-0461-2026)Philips Medical Systems DMC GmbH2025-11-07
CombiDiagnost R90; Model Number: 709031; recall (Z-0462-2026)Philips Medical Systems DMC GmbH2025-11-07
Precision CRF; Model Number: 706400; recall (Z-0463-2026)Philips Medical Systems DMC GmbH2025-11-07
DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 712031, (2) 7120 recall (Z-0464-2026)Philips Medical Systems DMC GmbH2025-11-07
DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 71203 recall (Z-0465-2026)Philips Medical Systems DMC GmbH2025-11-07
Radiography 7300 C; Model Number: 712037; recall (Z-0466-2026)Philips Medical Systems DMC GmbH2025-11-07
ProxiDiagnost N90. radiography and fluoroscopy system recall (Z-1325-2022)Philips Medical Systems DMC GmbH2022-07-12
DigitalDiagnost 4 High Performance. radiography and fluoroscopy system recall (Z-1326-2022)Philips Medical Systems DMC GmbH2022-07-12
DigitalDiagnost 4 Flex / Value. radiography and fluoroscopy system recall (Z-1327-2022)Philips Medical Systems DMC GmbH2022-07-12
DigitalDiagnost C90 High Performance. radiography and fluoroscopy system recall (Z-1328-2022)Philips Medical Systems DMC GmbH2022-07-12
DigitalDiagnost C90 Flex/Value/Chest/ER. radiography and fluoroscopy system recall (Z-1329-2022)Philips Medical Systems DMC GmbH2022-07-12

Track Philips Medical Systems DMC GmbH automatically

Every clearance here is in the API, with alerts when new ones post.