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 13, 2026, FDA's public records list Modern Diagnostics, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Oct 3, 1985: PREGNA/TEST.
| Date | Record | Source |
|---|---|---|
| Oct 3, 1985 | PREGNA/TESTK853269 · LCX | 510(k) clearances |
| Oct 1, 1985 | BETA-HCG MICROTITER PREGNANCY TESTK853258 · JHI | 510(k) clearances |
| Sep 4, 1985 | HUMAN CHORIONIC GONAD TEST SYS FOR EARLY PREGNANCYK853006 · JHI | 510(k) clearances |
| Aug 1, 1985 | ENZYME ANTINUCLEAR ANTIBODY SCREENING TESTK852840 · LJM | 510(k) clearances |
| May 15, 1985 | ANTINUCLEAR ANTIBODY TEST KITK851369 · DHN | 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
