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 Cardiac Resuscitator Corp. with 17 510(k) clearances. The most recent is a 510(k) clearance dated Jul 12, 1988: MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATOR.
| Jul 12, 1988 | MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATORK882513 · DSI | 510(k) clearances |
| Jun 24, 1987 | STAT-PAD (TM)K871538 · DRO | 510(k) clearances |
| Jun 24, 1987 | MODIFIED PACE*AID MODEL 53K871971 · DRO | 510(k) clearances |
| Jun 8, 1987 | MODIFIED HEART*AID 97 AUTO. EXTERNAL DEFIBRILLATORK871569 · DRO | 510(k) clearances |
| Apr 10, 1987 | HEART*AID 1000K870622 · MKJ | 510(k) clearances |
| Mar 6, 1985 | PACE*AID 10 A -PAD 10A- PACEMAKER OUTPUT DISPLAY &K850596 · DRO | 510(k) clearances |
| Feb 14, 1985 | HEART AID MODEL 97K850170 · DRO | 510(k) clearances |
| Jan 24, 1985 | PACE AID MODEL 53K844811 · DRO | 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
