Company ยท US
Technia Diagnostics , Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 1979 to 1986. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| CDD | Radioassay, Vitamin B12 | 1 |
| CDP | Radioimmunoassay, Total Triiodothyronine | 1 |
| CDX | Radioimmunoassay, Total Thyroxine | 1 |
| CGR | Radioimmunoassay, Cortisol | 1 |
| JMF | Radioimmunoassay, Human Placental Lactogen | 1 |
| KHQ | Radioassay, Triiodothyronine Uptake | 1 |
| KTL | Anti-Dna Indirect Immunofluorescent Solid Phase | 1 |
| LCQ | Fluorescent Immunoassay Gentamicin | 1 |
| LCS | Radioimmunoassay, Digoxin (125-I) | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jun 10, 1986 | K861978 | AUTOFLUOR V Technia Diagnostics , Ltd. | KTL |
| Sep 16, 1980 | K801843 | T3(125) RADIOIMMUNOASSAY KIT Technia Diagnostics , Ltd. | CDP |
| Jun 20, 1980 | K801202 | DIGOXIN RADIOIMMUNOASSAY KIT Technia Diagnostics , Ltd. | LCS |
| Jun 9, 1980 | K801203 | CORTISOL RADIOIMMUNOASSAY KIT Technia Diagnostics , Ltd. | CGR |
| Aug 16, 1979 | K791361 | T3 UPTAKE RADIOIMMUNOASSAY KIT Technia Diagnostics , Ltd. | KHQ |
| Jun 28, 1979 | K790919 | HPL RIA KIT Technia Diagnostics , Ltd. | JMF |
| May 3, 1979 | K790495 | THYROXINE RIA KIT Technia Diagnostics , Ltd. | CDX |
| Feb 28, 1979 | K782024 | RIA KIT, VITAMIN B12 Technia Diagnostics , Ltd. | CDD |
| Jan 26, 1979 | K782025 | GENTAMICIN FLUROIMMUNASSAY KIT Technia Diagnostics , Ltd. | LCQ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||