FDA 510(k) Applications Submitted by HITACHI, LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K162902 | 10/17/2016 | ARIETTA Prologue Diagnostic Ultrasound system and Transducers | HITACHI, LTD. |
| K162583 | 09/15/2016 | ALOKA LISENDO 880 | HITACHI, LTD. |
| K060834 | 03/27/2006 | PROBEAT WITH MGCS | HITACHI, LTD. |
| K161163 | 04/25/2016 | PROBEAT-V Proton Beam Therapy System with X-ray Limiting Accessory | HITACHI, LTD. |
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