Guangdong Biolight Meditech Co., Ltd.
FDA 510(k) medical device clearances.
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.