FDA 510(k) FDA unclassified Substantially Equivalent 🇯🇵 Japan

SANGRAY

K Number: K172087 · Decision Oct 27, 2017
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
15
Applicant Total
8
Review Days
108

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SANGRAY
K Number
K172087
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hitachi , Ltd.
Date Received
July 11, 2017
Decision Date
October 27, 2017
Product Code
MOT
Advisory Committee
Unknown
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MOT Irradiator, Blood To Prevent Graft Versus Host Disease

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MOT), ordered by most recent decision date.

View all

Other Clearances by Hitachi , Ltd.

K Number Device Name
K201042 PROBEAT-CR
K191801 PROBEAT-CR
K163505 ARIETTA PRECISION
K162902 ARIETTA Prologue Diagnostic Ultrasound system and Transducers
K162583 ALOKA LISENDO 880
K161163 PROBEAT-V Proton Beam Therapy System with X-ray Limiting Accessory
K060834 PROBEAT WITH MGCS