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Data / Medical devices / China / Foshan Mic Medical Technology Co., Ltd

Foshan Mic Medical Technology Co., Ltd: FDA-registered device maker in Foshan Guangdong, China, 1 510(k) clearance

Foshan Mic Medical Technology Co., Ltd is registered with the FDA (registration 3023245116) in Foshan Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 8, 2022. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
3023245116
Address
Bldg 6, Runzhi Sci-Tech Park, No.2 Taishan Rd, Guicheng, Nanhai Dist, Foshan Guangdong, China, 528200
Owner or operator
Foshan MIC Medical Technology Co., LTD (10084965)
Roles
Manufacturer
First device listed
April 21, 2022
Registered through
2027
Brand names listed
OXYGEN CONCENTRATOR (models: CP501, CP502, CP503, CP505, CP101)

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
April 8, 2022K202389Oxygen ConcentratorCAWSubstantially EquivalentFoshan Mic Medical Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated April 8, 2022. 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.