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Data / Medical devices / China / Neusoft Positron Medical Systems Co.,ltd.

Neusoft Positron Medical Systems Co.,ltd.: FDA-registered device maker in Shen Yang Liaoning, China, 1 510(k) clearance

Neusoft Positron Medical Systems Co.,ltd. is registered with the FDA (registration 3007675950) in Shen Yang Liaoning, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 24, 2009. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3007675950
Address
No.177-2, Chuangxin Road, Hunnan District, Shen Yang Liaoning, China, 110167
Owner or operator
Neusoft Positron Medical Systems Co LTD (10029410)
Roles
Manufacturer
First device listed
May 11, 2009
Registered through
2026
Brand names listed
Attrius, Attrius L, Truesight

Devices it lists

DeviceProduct codeClassRoleSource
System, Tomography, Computed, EmissionKPS2Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
April 24, 2009K090178ATTRIUS, MODEL PET150A6001, ATTRIUS L, MODEL PET150A8001, TRUESIGHT, MODEL NSP-P6C, TRUESIGHT, MODEL NSP-P8KPSSubstantially EquivalentNeusoft Positron Medical Systems Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated April 24, 2009. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.