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-Number | Device | Date |
| K781911 | ECG ANALYZER, HIGH SPEED | November 30, 1978 |
| K781514 | ECG ELECTRODE, 2021, 2022, 2032, 2033 | October 17, 1978 |
| K781152 | ELECTROCARDIOGRAPHIC ECG RECORDER | August 31, 1978 |
| K770988 | FOAM ECG ELECTRODE, 2060 AND 2061 | June 14, 1977 |