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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 8 of 8 Results
510(K) Number: K163210
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CombiDiagnost R90 1.0 (709030) 2 02/14/2024 PHILIPS MEDICAL SYSTEMS
CombiDiagnost R90 R.1.0 2 05/15/2023 Philips North America
CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 709030 and 709031 2 04/10/2023 Philips North America Llc
ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 706100 and 706110 2 04/10/2023 Philips North America Llc
CombiDiagnost GCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, ... 2 02/20/2020 Philips Medical Systems Gmbh, DMC
CombiDiagnost PCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, ... 2 02/20/2020 Philips Medical Systems Gmbh, DMC
Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030 Stationary Fluoroscopic X-ra... 2 02/12/2019 Philips Medical Systems Gmbh, DMC
CombiDiagnost R90 Image-Intensified fluoroscopic x-ray system CombiDiagnost R90 is a multi-functi... 2 01/10/2018 Philips Electronics North America Corporation
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