Cardio-Dynamics Laboratories, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K781911ECG ANALYZER, HIGH SPEEDNovember 30, 1978
K781514ECG ELECTRODE, 2021, 2022, 2032, 2033October 17, 1978
K781152ELECTROCARDIOGRAPHIC ECG RECORDERAugust 31, 1978
K770988FOAM ECG ELECTRODE, 2060 AND 2061June 14, 1977