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C-Arm Fluoroscopic X-Ray System

FDA product code RCC · Class 2 · Radiology

0
Registered devices
76
Adverse events
1
Recalls
0
510(k) clearances

Recent recalls

DateFirmReason
2020-05-08Ge HealthcareGEHC Surgery became aware that some users of the 9800 and 9900 fluoroscopic mobile C-Arms (referred to as the system here on) within the United States had reque

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.