Daesung Maref Co., Ltd.
Daesung Maref Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2023.
Top product codes for Daesung Maref Co., Ltd.
Recent clearances by Daesung Maref Co., Ltd.
- K231437 — LF900
- K202395 — SP-1000, SP-2000
- K203498 — LX9max
- K203019 — LF900
- K203353 — DVT-PRO
- K203417 — DVT-4000S
- K203016 — DVT-2600
- K160178 — Lympha-Flow(LF1200)
- K160180 — Intermittent Pneumatic Compression system
- K150980 — Venous Assist System
- K150033 — Air Compressible Limb Therapy System
- K112441 — COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM
- K112677 — THE VENOUS ASSIST SYSTEM
- K102320 — COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM MODEL LX7(V7)
Data sourced from openFDA. This site is unofficial and independent of the FDA.