Delta4 Phantom+ MR

The intended use of the device is • quality assurance of patient specific treatment delivery prior to the treatment in IMRT (including VMAT) and 4DRT (e.g. respiratory gating and tumour…

Registry build 21.09.26

The intended use of the device is • quality assurance of patient specific treatment delivery prior to the treatment in IMRT (including VMAT) and 4DRT (e.g. respiratory gating and tumour tracking). • quality assurance of the radiation delivery system.

8manufacturers in China registered for this device type
2catalogue numbers in this listing
5510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (2), Jiangsu (2), Beijing (2). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code IYE
Manufacturer City Province Registered as Device types
Guangzhou Tian Hong Medical Technology Co., Ltd. Guangzhou Guangdong Contract manufacturer 4
Klarity Medical & Equipment (GZ) Co., Ltd. Guangzhou Guangdong Contract manufacturer 3
Elekta Beijing Medical Systems Co., Ltd. Beijing Beijing Contract manufacturer 1
Manteia Technologies Co., Ltd. Xiamen Fujian Manufacturer 3
OUR United Corporation Xian Shaanxi Contract manufacturer 2
Suzhou Linatech Medical Science AND Technology Co., Ltd. Suzhou Jiangsu Manufacturer 2
Varian Medical Systems China Co., Ltd. Beijing Beijing Manufacturer 2
Jiangsu Rayer Medical Technology Co., Ltd. Wuxi Jiangsu Manufacturer 1

Record

Regulatory record for Delta4 Phantom+ MR
Listed by Scandidos AB, Sweden
FDA product code IYE
Device type Accelerator, Linear, Medical
Device class Class 2
Regulation 21 CFR 892.5050
510(k) K183606
Record published 2019-04-24

Specifications

Specifications
MRI safety MR Conditional
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Delta4 Phantom+ MR
Catalogue number Size Status
PMMA In distribution
PW In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Klarity Medical Klarity Medical Products, LLC 891
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Fibreplast® Qfix 271
Bionix Radiation Therapy Bionix Radiation Therapy, LLC 115
Vac-Lok™ Cushion Medtec LLC 100
Visicoil IZI Medical Products LLC 86
BodyFIX 3C-Medical Intelligence GmbH 84
AlignRT Plus Vision RT Limited 72
Fibreplast® Assure™ Open View Qfix 72
Accelerator, Linear, Medical PTW-Freiburg Physikalisch-Technische Werkstätten Dr. Pychlau GmbH 71
Thermoplastic Mask IZI Medical Products LLC 58

Showing 12 of 1,611. All products under Accelerator, Linear, Medical

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K223234 2024-01-16
K183606 2019-04-08
K151426 2016-01-29
K151180 2015-08-19
K052920 2006-01-12

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer