Diagnostics makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Diagnostic Reagent Technologies with 10 510(k) clearances. The most recent is a 510(k) clearance dated Oct 4, 1984: NEW ALLERG. COATED MICROFILTER WELL STRI.
| Oct 4, 1984 | NEW ALLERG. COATED MICROFILTER WELL STRIK843302 · DHB | 510(k) clearances |
| Nov 25, 1983 | POLYSTYRENE MICROTITER WELL IMMUNOSORK832345 · DGC | 510(k) clearances |
| Nov 21, 1983 | POLYSTYRENE MICROTITER PLATE IMMUNO-K832344 · DHB | 510(k) clearances |
| Nov 21, 1983 | POLYSTYRENE MICRO-LITER PLATE-BIRCHTREEK831984 · DGO | 510(k) clearances |
| Aug 8, 1983 | ALLERGEN IMMUNOSORBENTS IP SPECIFIC EK831496 · | 510(k) clearances |
| Jul 18, 1983 | LOGIPE A DATA REDUCSYSTEM IP SPECIFIC-K831774 · DGO | 510(k) clearances |
| Jun 2, 1983 | IP SPECIFIC GK830005 · DAA | 510(k) clearances |
| Apr 8, 1983 | POLYSTYRENE MICROTITER PLATE IMMUNOSORBK830653 · DGO | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
