Canberra Industries, 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 |
|---|
| K925265 | IMAGEVIEW 46000 | June 9, 1993 |
| K896202 | MATRIX(TM)-96 | January 2, 1990 |
| K834168 | FIBRINOGEN UPTAKE SYS -VARIOUS MODELS | December 29, 1983 |