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
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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 | Device Class | Medical Specialty |
|---|---|---|---|
| MOT | Irradiator, Blood To Prevent Graft Versus Host Disease | FDA unclassified | Unknown |
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|---|---|---|---|
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| K191801 | PROBEAT-CR | Sep 13, 2019 | Substantially Equivalent |
| K163505 | ARIETTA PRECISION | May 30, 2017 | Substantially Equivalent |
| K162902 | ARIETTA Prologue Diagnostic Ultrasound system and Transducers | Dec 15, 2016 | Substantially Equivalent |
| K162583 | ALOKA LISENDO 880 | Nov 17, 2016 | Substantially Equivalent |
| K161163 | PROBEAT-V Proton Beam Therapy System with X-ray Limiting Accessory | Jul 13, 2016 | Substantially Equivalent |
| K060834 | PROBEAT WITH MGCS | Apr 19, 2006 | Substantially Equivalent |