Contec Medical Systems Co.,Ltd
Contec Medical Systems Co.,Ltd holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2024, with 1 FDA device recall on record.
Top product codes for Contec Medical Systems Co.,Ltd
FDA recalls by Contec Medical Systems Co.,Ltd
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Contec Medical Systems Co.,Ltd
- K232893 — Pocket Fetal Doppler (CONTEC 10D), Pocket Fetal Doppler (CONTEC 10E), Pocket Fetal Doppler (CONTEC 10F)
- K232895 — B-Ultrasound Diagnostic System
- K232908 — Color Doppler Ultrasound Diagnostic System (CMS1700B), Color Doppler Ultrasound Diagnostic System (CMS1700C)
- K220245 — Pocket Fetal Doppler (Models CONTEC10C and CONTEC10CL)
- K202757 — CONTEC08A Electronic Sphygmomanometer, CONTEC08C Electronic Sphygmomanometer, ABPM50 Automatic Blood Pressure Monitor
- K201980 — Infrared Thermometer
- K171360 — CONTEC Electrocardiograph
- K170856 — CMS600P2 B-Ultrasound Diagnostic System
- K170954 — Portable ECG Monitor
- K152863 — Portable ECG Monitor
- K141362 — PULSE OXIMETER CMS50EW
- K110775 — ELECTRONIC SPHYGMOMANOMETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.