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 13, 2026, FDA's public records list Tago, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jun 1, 1984: TAGO FIFFU-GEN, OROSOMUCOID.
| Date | Record | Source |
|---|---|---|
| Jun 1, 1984 | TAGO FIFFU-GEN, OROSOMUCOIDK841734 · LKL | 510(k) clearances |
| May 22, 1984 | TAGO DIFFU-GEN C-REACTIVE PROTEINK841265 · DCN | 510(k) clearances |
| May 11, 1984 | DIFFU-GEN APOLIPOPROTEIN A-I RADIAL -K834218 · MSJ | 510(k) clearances |
| Mar 9, 1984 | DIFFU-GEN HAPTOGLOBIN RADIAL IMMUNOK840404 · DAD | 510(k) clearances |
| Nov 21, 1983 | TAGO DIFFU-GEN-APOLIPOPROTEIN B-100K833129 · MSJ | 510(k) clearances |
| Mar 24, 1983 | RA SCREENING TESTK830611 · DHR | 510(k) clearances |
| Mar 17, 1983 | MONO SCREENING TESTK830531 · KTN | 510(k) clearances |
| Feb 9, 1983 | HCG SCREENING TESTK830156 · JHJ | 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
