Technia Diagnostics , Ltd.
Technia Diagnostics , Ltd. 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 June 10, 1986.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K861978 | AUTOFLUOR V | June 10, 1986 |
| K801843 | T3(125) RADIOIMMUNOASSAY KIT | September 16, 1980 |
| K801202 | DIGOXIN RADIOIMMUNOASSAY KIT | June 20, 1980 |
| K801203 | CORTISOL RADIOIMMUNOASSAY KIT | June 9, 1980 |
| K791361 | T3 UPTAKE RADIOIMMUNOASSAY KIT | August 16, 1979 |
| K790919 | HPL RIA KIT | June 28, 1979 |
| K790495 | THYROXINE RIA KIT | May 3, 1979 |
| K782024 | RIA KIT, VITAMIN B12 | February 28, 1979 |
| K782025 | GENTAMICIN FLUROIMMUNASSAY KIT | January 26, 1979 |