SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION
6 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| Ceiling Type X-Ray Tube Support Models CH-200 and CH-200M used with RADspeed, SonialVision recall (Z-0499-2026) | SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION | 2025-11-13 |
| SONIALVISION G4 is a multi-purpose X-ray R/F system. The equipment is suitable for radiogr recall (Z-0316-2025) | SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION | 2024-11-07 |
| The FLUOROspeed is intended to be used as a universal diagnostic imaging system for radiog recall (Z-0317-2025) | SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION | 2024-11-07 |
| Trinias unity, Digital Angiography System with Catheterization Table, Model: KS-100 This s recall (Z-0139-2025) | SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION | 2024-10-22 |
| Shimadzu, Trinias, Digital Angiography System recall (Z-1292-2024) | SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION | 2024-03-14 |
| Over-Head Ceiling Tube Support, CH-200, CH-200M, Used with RadSpeed and RadSpeed PRO, Soni recall (Z-2270-2023) | SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION | 2023-07-31 |
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Every clearance here is in the API, with alerts when new ones post.