Diagnostics makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Cambridge Bioscience Corp. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Mar 15, 1989: HUMAN LYME EIA FOR THE DETECT OF ANTIBODIES.
| Date | Record | Source |
|---|---|---|
| Mar 15, 1989 | HUMAN LYME EIA FOR THE DETECT OF ANTIBODIESK890281 · LSR | 510(k) clearances |
| Jul 8, 1988 | ADENOCLONE(R)-TYPE 40/41 EIA DIAGNOSTIC TEST (48)K881894 · GOD | 510(k) clearances |
| Feb 24, 1988 | ADENOCLONE(TM)-EIA ADENOVIRUS ANTIGEN TESTK873082 · GOD | 510(k) clearances |
| Feb 24, 1988 | ADENOCLONE(TM)-IFA, ADENOVIRUS ANTIGEN TESTK873312 · GOD | 510(k) clearances |
| Nov 5, 1985 | ROTACLONE ROTAVIRUS DIAGNOSTIC KITK852969 · LIQ | 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
