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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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