Medical device 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 14, 2026, FDA's public records list Tech-Co, Inc. with 36 510(k) clearances. The most recent is a 510(k) clearance dated Jun 28, 1996: IN VITRO DIAGNOSTIC REAGENT SET, INDIR. PREG. TEST.
| Jun 28, 1996 | IN VITRO DIAGNOSTIC REAGENT SET, INDIR. PREG. TESTK921968 · JHJ | 510(k) clearances |
| Oct 1, 1992 | VISUAL HCG PREGNANCY TESTK923376 · JHI | 510(k) clearances |
| Apr 17, 1992 | T4 EIA BEAD ASSAYK920766 · CDX | 510(k) clearances |
| Mar 24, 1992 | DIRECT PREGNANCY TESTK920716 · JHJ | 510(k) clearances |
| Jul 10, 1990 | POTASSIUM REAGENT SETK902574 · CEJ | 510(k) clearances |
| May 17, 1990 | IRON/TOTAL IRON BINDING CAPACITYK901561 · JIY | 510(k) clearances |
| Oct 13, 1988 | ALANINE AMINO TRANSFERASE (COLORIMETRIC METHOD)K883387 · CKD | 510(k) clearances |
| Oct 6, 1988 | HEMOGLOBINK883683 · GJZ | 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
