Kemble Instruments, Inc.
Kemble Instruments, Inc. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 27, 1984.
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 |
| K832760 | RIA SOFTWARE | October 14, 1983 |
| K832734 | KEMTEK 400 RIA GAMMA COUNTER | 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 |