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Shimadzu Medical Systems

11 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANS recall (Z-2294-2026)Shimadzu Medical Systems2026-06-02
X-Ray Diagnostic Table, Model No. YSF-300 Use in combination with an X-ray high voltage ge recall (Z-1585-2016)Shimadzu Medical Systems2016-04-28
Shimadzu Digital Radiography X-Ray System, Catalog No. DAR-8000f. This device is intended recall (Z-1569-2014)Shimadzu Medical Systems2014-05-08
Mobile X-ray System, Model: MUX-100, MUX-100H Product Usage: The device is a mobile X-ray recall (Z-1150-2014)Shimadzu Medical Systems2014-03-07
Shimadzu Corporation - Mobile DaRt Evolution This device is a mobile X-ray system in order recall (Z-1369-2013)Shimadzu Medical Systems2013-06-03
R-30H , Diagnostic X-Ray Beam-Limiting Device. In combination with any of below X-ray tube recall (Z-0260-2013)Shimadzu Medical Systems2012-11-08
R-20J , Diagnostic X-Ray Beam-Limiting Device. In combination with any of below X-Ray tube recall (Z-0261-2013)Shimadzu Medical Systems2012-11-08
0.7U163CS-36 In combination with below systems MUX-100H, MUX-100D, MobileArt Evolution Bra recall (Z-0262-2013)Shimadzu Medical Systems2012-11-08
0.7/1.3U163CS-36 In combination with below systems MobileArt Evolution, MobileDaRt Evoluti recall (Z-0263-2013)Shimadzu Medical Systems2012-11-08
0.7/1.2JG326D-265 Product Usage: The device is a mobile X-ray system in order to take gene recall (Z-0264-2013)Shimadzu Medical Systems2012-11-08
0.4/0.7JG326D-265AX/AT Product Usage: The device is a mobile X-ray system in order to take recall (Z-0265-2013)Shimadzu Medical Systems2012-11-08

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