Guangdong Biolight Meditech Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Guangdong Biolight Meditech Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Patient Monitor
21
Total
21
Cleared
0
Denied
Guangdong Biolight Meditech Co., Ltd. has 21 FDA 510(k) cleared medical devices. Based in Shanghai, CN.
Historical record: 21 cleared submissions from 2008 to 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Guangdong Biolight Meditech Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mid-Link Consulting Co, Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Guangdong Biolight Meditech Co., Ltd.
21 devices
Cleared
Apr 05, 2019
Patient Monitor
Cardiovascular
261d
Cleared
May 24, 2017
Central Monitoring System
Cardiovascular
92d
Cleared
Jan 04, 2017
Truscope Ultra Patient Monitor
Cardiovascular
148d
Cleared
Nov 03, 2016
Electronic Sphygmomanometer
Cardiovascular
269d
Cleared
Sep 07, 2016
Central Monitoring System
Obstetrics & Gynecology
267d
Cleared
Feb 25, 2016
VITAL SIGNS MONITOR
Cardiovascular
118d
Cleared
Feb 09, 2016
Electronic Thermometer
General Hospital
139d
Cleared
Jan 06, 2016
Fingertip Pulse Oximeters M70, M70A, M70B, M70C, M70D
Anesthesiology
237d
Cleared
Jun 11, 2014
DIGITAL ELECTROCARDIOGRAPH
Cardiovascular
352d
Cleared
Jun 06, 2014
HANDHELD MONITOR
Cardiovascular
354d
Cleared
May 15, 2014
FETAL MONITORS
Obstetrics & Gynecology
322d
Cleared
Feb 18, 2014
A SERIES AND Q SERIES PATIENT MONITORS
Cardiovascular
238d