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Data / Medical devices / China / Shenyang Canta Medical Tech. Co., Ltd

Shenyang Canta Medical Tech. Co., Ltd: FDA-registered device maker in Shengyang Liaoning, China, 1 510(k) clearance

Shenyang Canta Medical Tech. Co., Ltd is registered with the FDA (registration 3007307467) in Shengyang Liaoning, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 27, 2008. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3007307467
Address
No. 2-1 Puyu Road, Shenbei New District, Shenyang, Liaoning Province, China, Shengyang Liaoning, China, 110136
Owner or operator
Shenyang Canta Medical Tech. Co., Ltd (10027198)
Roles
Manufacturer
First device listed
October 12, 2008
Registered through
2026
Brand names listed
HG5-W-NS Oxygen Concentrator, HG5-WN-NS Oxygen Concentrator

Devices it lists

DeviceProduct codeClassRoleSource
Generator, Oxygen, PortableCAW2Manufactureraccessdata.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 27, 2008K081508HG OXYGEN CONCENTRATOR, MODELS HG5-W & HG5-WNCAWSubstantially EquivalentShenyang Canta Medical Tech. Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated August 27, 2008. 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.