Guangdong Biolight Meditech Co., Ltd.
Guangdong Biolight Meditech Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2019.
Top product codes for Guangdong Biolight Meditech Co., Ltd.
Recent clearances by Guangdong Biolight Meditech Co., Ltd.
- K181919 — Patient Monitor
- K170514 — Central Monitoring System
- K162234 — Truscope Ultra Patient Monitor
- K160349 — Electronic Sphygmomanometer
- K153580 — Central Monitoring System
- K153135 — VITAL SIGNS MONITOR
- K152739 — Electronic Thermometer
- K151287 — Fingertip Pulse Oximeters M70, M70A, M70B, M70C, M70D
- K131858 — DIGITAL ELECTROCARDIOGRAPH
- K131762 — HANDHELD MONITOR
- K131941 — FETAL MONITORS
- K131898 — A SERIES AND Q SERIES PATIENT MONITORS
- K131763 — TRUSCOPE SERIES PATIENT MONITOR
- K120193 — ANY VIEW PATIENT MONITORS
- K113833 — VITAL SIGNS MONITOR
- K112804 — FINGERTIP PULSE OXIMETER
- K112803 — PATIENT MONITOR
- K102040 — PATIENT MONITOR
- K101694 — HANDHELD PULSE OXIMETER MODEL M800
- K100046 — M SEIRES PATIENT MONITOR MODEL M66, M69, M8000, M9000, M7000
- K081712 — FINGERTIP PULSE OXIMETER, MODEL M70, AND HANDHELD PULSE OXIMETER, MODEL M700
Data sourced from openFDA. This site is unofficial and independent of the FDA.