Kemble Instruments, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K842894 | KEMBLE 405 | August 27, 1984 |
| K832734 | KEMTEK 400 RIA GAMMA COUNTER | October 14, 1983 |
| K832760 | RIA SOFTWARE | October 14, 1983 |
| K832736 | KEMTEK 104 RIA GAMMA COUNTER | September 29, 1983 |
| K832735 | KEMTEK 103 RIA GAMMA COUNTER | September 29, 1983 |
| K830751 | KEMTEK 102 | April 6, 1983 |
| K822293 | IMMU-COUNT 404 | August 24, 1982 |
| K827748 | THYRO-COUNT THYROID UPTAKE SYSTEM 90IZD PROBE | August 16, 1982 |
| K820137 | IMMU-COUNT | February 5, 1982 |