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 Pulse Metric with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jan 10, 2002: DYNAPULSE 5200A PATHWAY BLOOD PRESSURE MONITORING SYSTEM.
| Jan 10, 2002 | DYNAPULSE 5200A PATHWAY BLOOD PRESSURE MONITORING SYSTEMK013478 · DXN | 510(k) clearances |
| Dec 13, 2001 | DYNAPULSE 5000A MINI ABP BLOOD PRESSURE MONITORING SYSTEMK013358 · DXN | 510(k) clearances |
| Nov 1, 2001 | DYNAPULSE 500G (DP500G) BLLOD PRESSURE MONITORING SYSTEMK012498 · DXN | 510(k) clearances |
| Jun 23, 1995 | DYNAPULSE 5000A (DP5000A)K945111 · DXN | 510(k) clearances |
| Jan 8, 1991 | DYNAPULSE 200MK904739 · 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
