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 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Cardiocom with 5 510(k) clearances. The most recent is a 510(k) clearance dated Aug 14, 2012: TABLET COMMANDER.
| Date | Record | Source |
|---|---|---|
| Aug 14, 2012 | TABLET COMMANDERK122285 · DRG | 510(k) clearances |
| Aug 25, 2009 | COMMANDER 111, MODEL CD300-CD399K091821 · DXN | 510(k) clearances |
| Dec 30, 2005 | CARDIOCOM COMMANDER IIIK053303 · DXN | 510(k) clearances |
| Dec 30, 2005 | COMMANDER III NON-INVASIVE BLOOD PRESSURE SYSTEMK053304 · DXN | 510(k) clearances |
| Nov 24, 2004 | COMMANDER IIK043096 · DXN | 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
