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 13, 2026, FDA's public records list Cardio Data with 6 510(k) clearances. The most recent is a 510(k) clearance dated Oct 11, 1985: CARDIO DATA PACERECORDER PR3.
| Date | Record | Source |
|---|---|---|
| Oct 11, 1985 | CARDIO DATA PACERECORDER PR3K853262 · DSH | 510(k) clearances |
| Feb 1, 1985 | CARDIO DATA MK4 HOLTER ANALYSIS SYSTEMK850136 · DSI | 510(k) clearances |
| Jan 30, 1984 | CARDIODATA PACE RECORDERK834257 · DSH | 510(k) clearances |
| May 9, 1983 | CARDIO DATA PACEMAKER RECORDERK831184 · DSH | 510(k) clearances |
| Aug 31, 1981 | CARDIO-DATA SYSTEM, #MARK IIIK812149 · DSI | 510(k) clearances |
| Feb 16, 1977 | PACEGUARDK770264 · DXH | 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
