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.

Cardio-Dynamics Laboratories, Inc.

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

Total Devices4

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K781911	ECG ANALYZER, HIGH SPEED	DSI	1978-11-30	View
510(k)	K781514	ECG ELECTRODE, 2021, 2022, 2032, 2033	DRX	1978-10-17	View
510(k)	K781152	ELECTROCARDIOGRAPHIC ECG RECORDER	DSM	1978-08-31	View
510(k)	K770988	FOAM ECG ELECTRODE, 2060 AND 2061	DRX	1977-06-14	View

↑