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Data / Medical devices / Gas Chromatograph, Carbon-Monoxide

Gas Chromatograph, Carbon-Monoxide (JKT): 4 FDA-registered makers in 2 countries

4 establishments in 2 countries are registered with the FDA to make Gas Chromatograph, Carbon-Monoxide (product code JKT, Class 1, 21 CFR 862.3220). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on April 28, 1983, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
JKT
Device class
1
Regulation
862.3220
Medical specialty
Clinical Toxicology

Makers by country

CountryMakers
China3
United Kingdom1

Makers of Gas Chromatograph, Carbon-Monoxide

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Infitek Co., Ltd.Shanghai, ChinaManufacturer0000api.fda.gov
Labpeak Co.,ltdJinan Shandong, ChinaExporter to the US, Manufacturer0000api.fda.gov
MD Diagnostics LtdChatham Kent, United KingdomManufacturer0000api.fda.gov
Scitek Global Co.,ltdJinan Shandong, ChinaExporter to the US, Manufacturer0000api.fda.gov

Updated April 28, 1983. 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.