Diagnostics 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 15, 2026, FDA's public records list Diagnostic Reagents, Inc. with 66 510(k) clearances. The most recent is a 510(k) clearance dated Nov 18, 1998: MODIFICATION OF TRICYCLIC SERUM TOX EIA ASSAY.
| Nov 18, 1998 | MODIFICATION OF TRICYCLIC SERUM TOX EIA ASSAYK983268 · LFH | 510(k) clearances |
| Nov 16, 1998 | NAPA EIA ASSAYK983812 · LAN | 510(k) clearances |
| Nov 12, 1998 | DIGOXIN IMMUNOASSAYK983323 · KXT | 510(k) clearances |
| Nov 6, 1998 | VANCOMYCIN EIA ASSAYK983280 · LEH | 510(k) clearances |
| Nov 5, 1998 | DRUGS OF ABUSE URINE CALIBRATORS AND CONTROLSK983159 · DKB | 510(k) clearances |
| Sep 12, 1997 | LIDOCAINE EIA ASSAYK973102 · KLR | 510(k) clearances |
| Aug 28, 1997 | 50NG/ML COCAINE METABOLITE CALIBRATORK972835 · DLJ | 510(k) clearances |
| Aug 4, 1997 | METHADONE EIA ASSAYK972526 · 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
