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Data / Medical devices / Japan / Medikit Co., Ltd.

Medikit Co., Ltd.: FDA-registered device maker in BUNKYO KU Tokyo, Japan, 3 510(k) clearances

Medikit Co., Ltd. is registered with the FDA (registration 3003184529) in BUNKYO KU Tokyo, Japan. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated September 20, 2019. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3003184529
Address
1-13-2 Yushima, BUNKYO KU Tokyo, Japan, 113-0034
Owner or operator
TOGO MEDIKIT CO., LTD. (8030371)
Roles
Exporter to the US
First device listed
September 12, 2014
Registered through
2026
Brand names listed
Supercath 5, Supercath5

Devices it lists

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
September 20, 2019K190001Supercath 5FOZSubstantially EquivalentTogo Medikit Co., Ltd.accessdata.fda.gov
March 23, 2018K172496SUPERCATH 5 (26G)FOZSubstantially EquivalentTogo Medikit Co., Ltd.accessdata.fda.gov
May 12, 2014K140419SUPERCATH5FOZSubstantially EquivalentTogo Medikit Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated September 20, 2019. 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.