Philips Medical Systems GmbH, Dmc
Philips Medical Systems GmbH, Dmc holds FDA 510(k) medical device clearance, cleared in 2007, with 33 FDA device recalls on record.
Top product codes for Philips Medical Systems GmbH, Dmc
FDA recalls by Philips Medical Systems GmbH, Dmc
10 most recent of 33- Z-2357-2021 — CombiDiagnost R90 Software Version R1.0 and R1.1
- Z-1329-2020 — CombiDiagnost PCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic, general purpose.
- Z-1328-2020 — CombiDiagnost GCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic, general purpose.
- Z-0612-2019 — Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030 Stationary Fluoroscopic X-ray System
- Z-0239-2019 — Philips DigitalDiagnost software 4.1.x and 4.2.x, A Stationary X-ray System Models: 712027, 712028, 712029, 712031, 712032701032, 712033, 712224, 712225, 712226, 712227, 712228.
- Z-2843-2018 — DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031
- Z-2867-2018 — EasyDiagnost Eleva DRF (Stitching Patient Support) 706032
- Z-2851-2018 — DigitalDiagnost 4 High Performance (Stitching Patient Support) 712027
- Z-2849-2018 — DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029
- Z-2863-2018 — DigitalDiagnost Single Detector (Stitching Patient Support) 712020
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 GmbH, Dmc
Data sourced from openFDA. This site is unofficial and independent of the FDA.