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 Instruments with 8 510(k) clearances. The most recent is a 510(k) clearance dated Feb 26, 1990: EKG, ECG KENZ, ECG 302.
| Feb 26, 1990 | EKG, ECG KENZ, ECG 302K896771 · DSI | 510(k) clearances |
| Feb 26, 1990 | EKG, ECG KENZ, ECG 303K896772 · DPS | 510(k) clearances |
| Jan 4, 1990 | MODEL MC6500 ELECTROCARDIOGRAPHK895961 · DSH | 510(k) clearances |
| Jan 25, 1989 | MC6700 MULTI-CHANNEL ELECTROCARDIOGRAPHK883454 · DPS | 510(k) clearances |
| Nov 23, 1987 | MC 6000 MULTI-CHANNEL ELECTROCARDIOGRAPHK871993 · DPS | 510(k) clearances |
| Aug 25, 1986 | MODEL SC-1000 ELECTROCARDIOGRAPH SPECIFICATIONK862748 · DPS | 510(k) clearances |
| Jan 8, 1986 | PREVIEW XTK854282 · DSI | 510(k) clearances |
| Nov 13, 1985 | CAMBRIDGE MODEL XT1000K854283 · IOL | 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
