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 Micromedical Industries with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jan 3, 2002: MODIFICATION TO: POCKETVIEW ECG SOFTWARE.
| Jan 3, 2002 | MODIFICATION TO: POCKETVIEW ECG SOFTWAREK013311 · MHX | 510(k) clearances |
| Sep 26, 2001 | BLY-501 ADAPTORK012540 · DPS | 510(k) clearances |
| Feb 2, 1999 | MICROMEDICAL 12 LEAD SIMULTANEOUS CABLEK990266 · LOS | 510(k) clearances |
| May 12, 1995 | CMS SYSTEMK922528 · DQK | 510(k) clearances |
| Mar 27, 1992 | MODIFIED BIOLOGK915624 · DRT | 510(k) clearances |
| Mar 27, 1992 | PACEVIEWK915627 · KRB | 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
