Hitachi , Ltd.

Hitachi , Ltd. holds 8 FDA 510(k) medical device clearances, first cleared 2006, most recent 2020.

Top product codes for Hitachi , Ltd.

Recent clearances by Hitachi , Ltd.

K201042 — PROBEAT-CRCode LHN·2020-07-13
K191801 — PROBEAT-CRCode LHN·2019-09-13
K172087 — SANGRAYCode MOT·2017-10-27
K163505 — ARIETTA PRECISIONCode IYN·2017-05-30
K162902 — ARIETTA Prologue Diagnostic Ultrasound system and TransducersCode IYN·2016-12-15
K162583 — ALOKA LISENDO 880Code IYN·2016-11-17
K161163 — PROBEAT-V Proton Beam Therapy System with X-ray Limiting AccessoryCode LHN·2016-07-13
K060834 — PROBEAT WITH MGCSCode LHN·2006-04-19

Data sourced from openFDA. This site is unofficial and independent of the FDA.