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Arineta , Ltd.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories1
Latest FDA decision2025-04-15
TypeNumberDevice NameCodeDateActions
510(k) K250650 SpotLight / SpotLight Duo with Low Dose Lung Cancer Screening OptionJAK2025-04-15 View
510(k) K241200 SpotLight/SpotLight Duo with Low Dose Lung Cancer Screening OptionJAK2025-01-13 View
510(k) K230370 SpotLight/SpotLight Duo (with DLIR option)JAK2023-10-13 View
510(k) K213465 CardioGrapheJAK2022-12-02 View
510(k) K161066 SpotLight CTJAK2016-08-10 View
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