Bionet Co., Ltd. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Bionet Co., Ltd. has 11 FDA 510(k) cleared medical devices. Based in Wonju, Kwangwon-Do, KR.
Last cleared in 2023. Active since 2005. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Bionet Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Bionet Co., Ltd.
11 devices
Cleared
Dec 15, 2023
Cardio Q50, Cardio Q70
Cardiovascular
238d
Cleared
Nov 09, 2023
Cardio P1
Cardiovascular
202d
Cleared
Nov 15, 2022
Cardio10
Cardiovascular
264d
Cleared
Oct 11, 2022
SonoMe Wireless Probe Type Ultrasound Scanner (Model: 5C, 5CB, H5C, 10L, 14L,...
Radiology
264d
Cleared
Nov 15, 2013
SPM-300
Anesthesiology
280d
Cleared
Jul 16, 2012
CARDIO 7
Cardiovascular
250d
Cleared
Jun 03, 2011
CARDIO XP
Cardiovascular
252d
Cleared
Aug 26, 2009
EKG-PLUS II SOFTWARE
Cardiovascular
149d
Cleared
Dec 11, 2008
BIONET BM3PLUS PATIENT MONITOR
Cardiovascular
149d
Cleared
Dec 16, 2005
FC 700 FETAL MONITOR
Obstetrics & Gynecology
352d
Cleared
Dec 16, 2005
FC 1400 FETAL MONITOR
Obstetrics & Gynecology
352d