Diagnostics makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United KingdomLabelled 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 Cozart Bioscience with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jun 3, 2004: COZART EIA AMPHETAMINES ORAL FLUID MICROPLATE KIT.
| Jun 3, 2004 | COZART EIA AMPHETAMINES ORAL FLUID MICROPLATE KITK033743 · DKZ | 510(k) clearances |
| May 14, 2003 | COZART EIA COTININE URINE KITK021944 · MKU | 510(k) clearances |
| Apr 28, 2003 | COZART EIA COCAINE ORAL FLIUD KITK030234 · DIO | 510(k) clearances |
| Apr 7, 2003 | COZART EIA OPIATES ORAL FLUID KITK024339 · DIG | 510(k) clearances |
| Nov 5, 2002 | COZART RAPISCAN ORAL FLUID DRUG TEST - OPIATE/METHADONEK020920 · DJG | 510(k) clearances |
| Jul 31, 2001 | METHADONE MICROPLATE EIA URINE APPLICATIONK011131 · DJR | 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
