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 Lee Laboratories, Inc. with 10 510(k) clearances. The most recent is a 510(k) clearance dated Aug 25, 1997: VISTA ANTIGEN BRUCELLA ABORTUS.
| Aug 25, 1997 | VISTA ANTIGEN BRUCELLA ABORTUSK972394 · GSO | 510(k) clearances |
| Aug 25, 1997 | VISTA ANTIGEN SALMONELLA O GROUP AK972387 · GNC | 510(k) clearances |
| Aug 25, 1997 | VISTA ANTIGEN BRUCELLA MELITENSISK972396 · GSO | 510(k) clearances |
| Aug 25, 1997 | VISTA ANTIGEN SALMONELLA H DK972389 · GNC | 510(k) clearances |
| Aug 25, 1997 | VISTA ANTIGEN SALMONELLA H BK972391 · GNC | 510(k) clearances |
| Aug 25, 1997 | VISTA ANTIGEN SALMONELLA H CK972390 · GNC | 510(k) clearances |
| Aug 25, 1997 | VISTA ANTIGEN SALMONELLA O GROUP DK972395 · GNC | 510(k) clearances |
| Aug 25, 1997 | VISTA ANTIGEN SALMONELLA O GROUP CK972388 · GNC | 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
