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.

Non-Invasive Monitoring Systems, Inc.

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K012020 RESPIEVENTS SOFTWARE IS EVENT DATA PROCESSING SOFWARE FOR A PCDQK2001-08-21 View
510(k) K001369 RESPIEVENTS, VERSION 4.2DQK2000-07-26 View
510(k) K942852 RESPITRACE PTDQK1996-02-13 View
510(k) K942771 RESPIEVENTSDQK1996-02-13 View
510(k) K903011 RESPITRACE PLUS, RESPIBANDS, AND RESPICENTRALBZQ1991-03-29 View
510(k) K884959 RESPITRAKBZK1989-06-08 View
↑