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Data / Medical devices / China / Liaoning JRSD Commercial AND Trading Co.,Ltd.

Liaoning JRSD Commercial AND Trading Co.,Ltd.: FDA-registered device maker in Shenyang Liaoning, China, 1 510(k) clearance

Liaoning JRSD Commercial AND Trading Co.,Ltd. is registered with the FDA (registration 3015552886) in Shenyang Liaoning, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 25, 2017. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3015552886
Address
Room.801, No.5-2, Tianci Street Hunnan New District, Shenyang Liaoning, China, 110000
Owner or operator
Prosidio Inc (10081700)
Roles
Manufacturer
First device listed
April 23, 2022
Registered through
2026
Brand names listed
EJ-1/2/3/4, HiFi Rigid Sinuscopes

Devices it lists

DeviceProduct codeClassRoleSource
Nasopharyngoscope (Flexible Or Rigid)EOB2Manufactureraccessdata.fda.gov
OtoscopeERA1Manufactureraccessdata.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
August 25, 2017K161298ShenDa SinuscopeEOBSubstantially EquivalentShenyang Shenda Endoscope Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated August 25, 2017. 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.