Medical device 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 15, 2026, FDA's public records list Cardiac Control Systems, Inc. with 26 510(k) clearances. The most recent is a 510(k) clearance dated Dec 29, 1997: INTERIM AV SHAPED TEMPORARY PACING CATHETER MODEL INT-AV610.
| Dec 29, 1997 | INTERIM AV SHAPED TEMPORARY PACING CATHETER MODEL INT-AV610K971775 · LDF | 510(k) clearances |
| May 15, 1995 | CCDS MAESTRO(R) II SERIES 200 CADIAC PACEMAKERK946188 · DXY | 510(k) clearances |
| May 3, 1995 | CCS MAESTRO(R) II SERIES 200 MODELS 235 AND 227 CARDIAC PACEMAKERK950210 · DXY | 510(k) clearances |
| May 14, 1993 | CCS MAESTRO II SERIES 200 CARDIAC PACEMAKERK923868 · DXY | 510(k) clearances |
| May 16, 1991 | MAESTRO(R) SERIES 100/200 CARDIAC S/CHAMB PACEMAKEK905824 · DXY | 510(k) clearances |
| Jan 3, 1991 | MAESTRO SERIES 100/200 CARDIAC SINGLE CHAMBER PACEK904941 · DXY | 510(k) clearances |
| Sep 26, 1989 | MAESTRO PACEMAKER TEST MAGNETK895110 · DTG | 510(k) clearances |
| Oct 17, 1988 | MAESTRO(R) SERIES 100/200 SINGLE CHAMBER PACEMAKERK884023 · DXY | 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
