Guangzhou Minsheng Electronic Technical Co., Ltd. · 89-08 · CHINA
For Guangzhou Minsheng Electronic Technical Co., Ltd. · 89-08 · CHINA, import alert is 89-08; import alert name is "Detention Without Physical Examination of Devices without Approved PMA's or IDE's and Other Devices Not Substantially Equivalent or Without a 510(k)"; country is CHINA; product is Dr. Fargo Photon Energy Detoxification Bag; product code is 90 M - - UJ System, Planning, Radiation Therapy Treatment; date published is 11/03/2016; address is No. 8 Fenghe Road , Renhezhen Baiyun , Guangzhou, Guangdong CHINA, verified against its source on 2026-09-16.
- Firm
- Guangzhou Minsheng Electronic Technical Co., Ltd. verified
- Import alert
- 89-08
- Import alert name
- "Detention Without Physical Examination of Devices without Approved PMA's or IDE's and Other Devices Not Substantially Equivalent or Without a 510(k)"
- Country
- CHINA verified
- Address
- No. 8 Fenghe Road , Renhezhen Baiyun , Guangzhou, Guangdong CHINA verified
- Date published
- 11/03/2016 verified
- Product code
- 90 M - - UJ System, Planning, Radiation Therapy Treatment verified
- Product
- Dr. Fargo Photon Energy Detoxification Bag verified
- FDA notes
- Class II Device (may be a Class III). The device claims made are varied and the mechanism of technology of the device is and it is unclear how the device produces the intended effects are unclear. CDRH is not aware of any predicate devices that the manufacturer may compare to for 510(k) submission. Therefore; there is no specific product code or regulation that applies to this device since there are no known predicate device(s). verified
What the source says
Guangzhou Minsheng Electronic Technical Co., Ltd. Date Published : 11/03/2016 No. 8 Fenghe Road , Renhezhen Baiyun , Guangzhou, Guangdong CHINA 90 M - - UJ System, Planning, Radiation Therapy Treatment Date Published: 11/03/2016 Desc: Dr. Fargo Photon Energy Detoxification Bag Notes: Class II Device (may be a Class III). The device claims made are varied and the mechanism of technology of the device is and it is unclear how the device produces the intended effects are unclear. CDRH is not aware of any predicate devices that the manufacturer may compare to for 510(k) submission. Therefore; there is no specific product code or regulation that applies to this device since there are no known predicate device(s).
— accessdata.fda.gov, retrieved 2026-09-15
Source
- accessdata.fda.govhttps://www.accessdata.fda.gov/cms_ia/importalert_244.html
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