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 Tudor Laboratories with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jun 24, 1992: THYROXINE (FPIA) KIT.
| Jun 24, 1992 | THYROXINE (FPIA) KITK921904 · KLI | 510(k) clearances |
| May 26, 1992 | THYROXINE CALIBRATOR KITK921903 · JIS | 510(k) clearances |
| Sep 6, 1991 | DIGITOXIN (FPIA) KITK913240 · LFM | 510(k) clearances |
| Oct 30, 1989 | N-ACETYLPROCAINAMIDE (NAPA) CALIBRATOR KITK895572 · DLJ | 510(k) clearances |
| Oct 25, 1989 | N-ACETYLPROCAINAMIDE (NAPA) (FPIA) KITK895571 · LAN | 510(k) clearances |
| Oct 20, 1989 | PRIMIDONE (FPIA) KITK895567 · LFT | 510(k) clearances |
| Oct 3, 1989 | VALPROIC ACID (FPIA) KITK895569 · LEG | 510(k) clearances |
| Sep 28, 1989 | VALPROIC ACID (FPIA) CALIBRATOR KITK895570 · DLJ | 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
