Clinical Data Instruments, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K842349 | AMBULATORY PH RECORDING DEVICE | June 14, 1985 |
| K832828 | CENTURION CARDIAC DETECTOR | May 9, 1984 |
| K832829 | NEO-FLOAT NEONATAL FLOTATION SYS & RHYT | October 4, 1983 |