Pharmaceutical companyLabelled 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 Kent Laboratories with 40 510(k) clearances. The most recent is a 510(k) clearance dated Jun 1, 1995: HUMAN PREALBUMIN RADIAL IMMUNODIFFUSION KIT.
| Jun 1, 1995 | HUMAN PREALBUMIN RADIAL IMMUNODIFFUSION KITK951966 · JZJ | 510(k) clearances |
| May 30, 1995 | HUMAN C1 INACTIVATOR OR C-1 ESTERASE INHIBITOR RADIAL IMMUNODIFFUSION KITK951967 · DBA | 510(k) clearances |
| May 30, 1995 | HUMAN C1Q RADIAL IMMUNODIFFUSION KITK951968 · DAK | 510(k) clearances |
| Apr 10, 1995 | HUMAN C-5 RADIAL IMMUNODIFFUSION KITK950102 · DAY | 510(k) clearances |
| Nov 27, 1985 | 72 DETERM. SIZE RADIAL IMMUNODIFFUSION TEST ALPHA2K850683 · DEB | 510(k) clearances |
| Nov 25, 1985 | 72 DETERM. SIZE RADIAL IMMUNO. TEST HUMAN CERULOPLK850682 · DDB | 510(k) clearances |
| Nov 1, 1985 | ANTISERUM TO HUMAN PREALBUMINK850686 · JZJ | 510(k) clearances |
| Nov 1, 1985 | ANTISERUM TO HUMAN APOLIPOPROTEIN BK850690 · MSJ | 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
