Bionet Co., Ltd.
Bionet Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2023.
Top product codes for Bionet Co., Ltd.
Recent clearances by Bionet Co., Ltd.
- K231160 — Cardio Q50, Cardio Q70
- K231150 — Cardio P1
- K220535 — Cardio10
- K220169 — SonoMe Wireless Probe Type Ultrasound Scanner (Model: 5C, 5CB, H5C, 10L, 14L, 10LB, H10L, H5C10L) and SonoFinder Wireless Probe Type Ultrasound Scanner (Model: SF14L25)
- K130322 — SPM-300
- K113306 — CARDIO 7
- K102767 — CARDIO XP
- K090895 — EKG-PLUS II SOFTWARE
- K082008 — BIONET BM3PLUS PATIENT MONITOR
- K043597 — FC 700 FETAL MONITOR
- K043598 — FC 1400 FETAL MONITOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.