Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Coreline Soft Co., Ltd.

FDA 510(k) & PMA Approved Devices — 12 products

Total Devices12
Categories4
Latest FDA decision2025-12-03
TypeNumberDevice NameCodeDateActions
510(k) K251203 AVIEW Lung Nodule CADOEB2025-12-03 View
510(k) K243689 AVIEWQIH2025-03-19 View
510(k) K243696 AVIEW CACQIH2025-02-14 View
510(k) K233211 AVIEW CACQIH2024-03-29 View
510(k) K221592 AVIEW Lung Nodule CADOEB2023-02-24 View
510(k) K214036 AVIEWQIH2022-12-23 View
510(k) K220408 AVIEW RT ACSQKB2022-11-10 View
510(k) K201710 A View LCSLLZ2020-10-16 View
510(k) K200714 AVIEWLLZ2020-08-26 View
510(k) K193220 AVIEW LCSLLZ2020-05-05 View
510(k) K192040 AVIEW ModelerLLZ2019-12-20 View
510(k) K171199 AVIEWLLZ2018-10-31 View