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.

Cardionostics, Inc.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K902486	CARDIOVISTA	DSH	1990-08-23	View
510(k)	K863863	CARDIONOSTICS HOLTER DURA-LITE RECORDER (CASSETTE)	DSH	1986-10-15	View
510(k)	K844977	HOLTER CURA-LITE RECORDER	DSH	1985-01-14	View
510(k)	K842954	CARDIONOSTICS HOLTER DURA-LITE RECORDE	DSH	1984-09-04	View

↑