Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Nipro Diagnostics, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K132072 TRUE METRIX SELF-MONITORING BLOOD GLUCOSE SYSTEM, TRUE METRI PRO PROFESSIONAL MONITORING BLOOD GLUCOSE SYSTEMNBW2013-08-15 View
510(k) K120989 TRUE METRIX SELF-MONITORING BLOOD GLUCOSE SYSTEM, TRUE METRIX PROFESSIONAL MONITORING BLOOD GLUCOSE SYSTEMNBW2013-04-24 View
↑