Medical device 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 Cambridge Medical Technology with 14 510(k) clearances. The most recent is a 510(k) clearance dated Apr 26, 1989: RIA-GNOST INSULIN.
| Apr 26, 1989 | RIA-GNOST INSULINK890837 · CFP | 510(k) clearances |
| Mar 16, 1989 | RIA-GNOST PROGESTERONEK890836 · JLS | 510(k) clearances |
| Mar 16, 1989 | RIA-GNOST FERRITINK890697 · JMG | 510(k) clearances |
| Nov 24, 1987 | NO SPIN(TM) T3 COATED TUBE RADIOIMMUNOASSAYK873737 · CDP | 510(k) clearances |
| Apr 22, 1987 | T4 NO SPIN(TM) COATED TUBE RADIOIMMUNOASSAY KITK870573 · CDX | 510(k) clearances |
| Aug 19, 1986 | RADIOIMMUNOASSAY OF NO SPIN(TM) CORTISOLK862871 · CGR | 510(k) clearances |
| Feb 19, 1986 | TESTOSTERONE COATED TUBES RADIOIMMUNOASSAY KITK860130 · CDZ | 510(k) clearances |
| Feb 6, 1986 | T3 UPTAKE RADIOIMMUNOASSAY KITK855169 · KHQ | 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
