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 13, 2026, FDA's public records list Cardiotronics with 27 510(k) clearances. The most recent is a 510(k) clearance dated Feb 24, 1995: EKG VEST.
| Date | Record | Source |
|---|---|---|
| Feb 24, 1995 | EKG VESTK932903 · DRX | 510(k) clearances |
| Dec 1, 1992 | MODEL #510 STEALTH-PLATE DISPERSIVE ELECTRODEK922064 · GXD | 510(k) clearances |
| Sep 18, 1992 | MODEL #340 STEALTH-TRODE+LSK923297 · LDD | 510(k) clearances |
| Jun 11, 1992 | MODEL # 230 ST STEALTH-TRODE DEFIB PADS (STERILE)K922172 · LDD | 510(k) clearances |
| Jun 11, 1992 | MODEL # 830 ST ADULT STIMULATION PADS (STERILE)K922173 · LDD | 510(k) clearances |
| Jun 11, 1992 | MODEL #225-ST SHOCK-TRODE ADULT DEFIB PADS STERILEK922227 · LDD | 510(k) clearances |
| May 26, 1992 | MODEL #125 CHILD STIMULATION PADSK921606 · LDD | 510(k) clearances |
| Feb 3, 1992 | SHOCK-PATCH ADULT DEFIBRILLATION PADSK920086 · LDD | 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
