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 Corventis with 7 510(k) clearances. The most recent is a 510(k) clearance dated Feb 6, 2014: NUVANT MCT SYSTEM.
| Date | Record | Source |
|---|---|---|
| Feb 6, 2014 | NUVANT MCT SYSTEMK133701 · QYX | 510(k) clearances |
| Mar 7, 2012 | NUVANT, MOBILC CARDIAC TELEMETRYK113372 · QYX | 510(k) clearances |
| Jan 4, 2012 | AVIVO MOBILE PATIENT MANAGEMENTK113187 · MHX | 510(k) clearances |
| Aug 24, 2011 | NUVANT, MOBILE CARDIAC TELEMETRYK111917 · QYX | 510(k) clearances |
| Aug 27, 2009 | AVIVO MOBILE PATIENT MANAGEMENT SYSTEM, NUVANT MOBILE CARDIAC TELEMETRY (MCT) SYSTEMK091971 · DSI | 510(k) clearances |
| Jun 19, 2009 | NUVANT CARDIAC EVENT MONITORING SYSTEM; NUVANT MOBILE CARDIAC TELEMETRY SYSTEMK090696 · QYX | 510(k) clearances |
| Feb 3, 2009 | AVIVO MOBILE PATIENT MANAGEMENT SYSTEMK083287 · DSI | 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
