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 13, 2026, FDA's public records list Photec Diagnostics with 12 510(k) clearances. The most recent is a 510(k) clearance dated Feb 23, 1990: QUIKREAD(R) WHOLE BLOOD TRIGLYCERIDE TEST KIT.
| Feb 23, 1990 | QUIKREAD(R) WHOLE BLOOD TRIGLYCERIDE TEST KITK897169 · CDT | 510(k) clearances |
| Dec 12, 1989 | D-CHEM TOTAL T4 TEST KIT FOR THYROXINE QUANTITA.K896329 · KLI | 510(k) clearances |
| Aug 31, 1989 | QUIKREAD WHOLE BLOOD HDL-CHOLESTEROL TEST KITK894057 · LBS | 510(k) clearances |
| Jun 16, 1989 | D-CHEM(TM) T-UPTAKE TEST KIT FOR T-UPTAKE DETERMINK892224 · KHQ | 510(k) clearances |
| Apr 26, 1989 | QUIKREAD CHEM. ANALYZER & CHOLES. FOR SERUM/PLASMAK890267 · CHH | 510(k) clearances |
| Apr 26, 1989 | QUIKREAD CHEM. ANALYZER & CHOLES. FOR WHOLE BLOODK890027 · CHH | 510(k) clearances |
| Aug 2, 1988 | D-CHEMK882307 · JJE | 510(k) clearances |
| Mar 24, 1988 | THEOPHYLLINE TEST KIT REF. #A874799K880291 · LCA | 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
