Contec Medical System Co., Ltd.
Contec Medical System Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2019.
Top product codes for Contec Medical System Co., Ltd.
Recent clearances by Contec Medical System Co., Ltd.
- K180837 — CONTEC Oxygen Concentrator
- K131900 — CONTEC ELECTROCARDIOGRAPH
- K101273 — DYNAMIC ECG SYSTEM MODEL TLC5000
- K110156 — AMBULATORY BLLOD PRESSURE MONITOR, ELECTRONIC SPHYGMOMANOMETER,
- K101692 — PATIENT MONITOR
- K110774 — ELECTRONIC SPHYGMOMANOMETER
- K101127 — PATIENT MONITOR, MODEL PM50
- K090936 — SINGLE-CHANNEL HANDHELD ELECTROCARDIOGRAPH, MODEL ECG80A
- K090671 — PULSE OXIMETER, MODELS CMS50E, CMS50F, CMS60C, CMS60D
- K082480 — CONTEC POCKET FETAL DOPPLER
- K082641 — FINGERTIP PULSE OXIMETER, MODELS CMS-50D, CMS-50L, CMS-50DL
- K073454 — FINGERTIP PULSE OXIMETER, MODEL CMS-50C
Data sourced from openFDA. This site is unofficial and independent of the FDA.