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., part of Laerdal MedicalLabelled 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 Laerdal Mfg. Corp. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Sep 27, 1990: MODIFIED HEARTSTART DEFIBRILLATION ELECTRODE.
| Sep 27, 1990 | MODIFIED HEARTSTART DEFIBRILLATION ELECTRODEK902429 · LDD | 510(k) clearances |
| Jan 26, 1990 | MODIFIED HEARTSTART 2000 DEFIBRILLATION ELECTRODEK900169 · LDD | 510(k) clearances |
| Feb 23, 1989 | HEARTSTART 2000 DEFIBRILLATION ELECTRODEK885186 · LDD | 510(k) clearances |
| Sep 12, 1988 | HEARTSTART 1000SK883344 · MKJ | 510(k) clearances |
| Sep 12, 1988 | HEARTSTART 1000K883341 · MKJ | 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
