Nipro Diagnostics, Inc. is one of 13039 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nipro Diagnostics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TRUE METRIX AIR Self-Monitoring Blood Glucose System, TRUE METRIX AIR PRO Professional Blood Gulcose Monitoring System, TRUE METRIX SELF-MONITORING BLOOD GLUCOSE SYSTEM, TRUE METRIX PRO PROFESSIONAL MONITORING BLOOD GLUCOSE SYSTEM, TRUE METRIX SELF-MONITORING BLOOD GLUCOSE SYSTEM, TRUE METRI PRO PROFESSIONAL MONITORING BLOOD GLUCOSE SYSTEM
4
Total
4
Cleared
0
Denied
Nipro Diagnostics, Inc. has 4 FDA 510(k) cleared medical devices. Based in Fort Lauderdale, US.
Historical record: 4 cleared submissions from 2013 to 2015. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Nipro Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nipro Diagnostics, Inc.
4 devices
Cleared
Mar 26, 2015
TRUE METRIX AIR Self-Monitoring Blood Glucose System, TRUE METRIX AIR PRO...
Chemistry
73d
Cleared
Aug 01, 2014
TRUE METRIX SELF-MONITORING BLOOD GLUCOSE SYSTEM, TRUE METRIX PRO...
Chemistry
198d
Cleared
Aug 15, 2013
TRUE METRIX SELF-MONITORING BLOOD GLUCOSE SYSTEM, TRUE METRI PRO PROFESSIONAL...
Chemistry
43d
Cleared
Apr 24, 2013
TRUE METRIX SELF-MONITORING BLOOD GLUCOSE SYSTEM, TRUE METRIX PROFESSIONAL...
Chemistry
387d