FDA 510(k) Applications Submitted by Daesung Maref Co., Ltd

FDA 510(k) Number Submission Date Device Name Applicant
K202395 08/21/2020 SP-1000, SP-2000 DaeSung Maref Co., Ltd
K160178 01/27/2016 Lympha-Flow(LF1200) DaeSung Maref Co., Ltd
K160180 01/27/2016 Intermittent Pneumatic Compression system DaeSung Maref Co., Ltd
K203019 10/01/2020 LF900 DaeSung Maref Co., Ltd
K231437 05/17/2023 LF900 Daesung Maref Co., Ltd
K203016 10/01/2020 DVT-2600 Daesung Maref Co., LTD
K203353 11/13/2020 DVT-PRO Daesung Maref Co., LTD


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