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 Harvard Medical Devices with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 2, 2010: FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR , MODEL KN-550.
| Jul 2, 2010 | FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR , MODEL KN-550K100620 · DXN | 510(k) clearances |
| Mar 17, 2010 | WRIST TYPE BLOOD PRESSURE MONITOR, HMBPM-005/KINETIK BRANDED BPM2 SERIESK092558 · DXN | 510(k) clearances |
| Dec 17, 2009 | DIGITAL THERMOMETER,HMCDT-002/KINETIK BRANDED DT1 SERIESK092557 · FLL | 510(k) clearances |
| Aug 8, 2008 | HARVARD MEDICAL DEVICES BLOOD PRESSURE MONITOR, MODEL HMBPM-004/KINETIK BRANDED BPM1 SERIESK081159 · DXN | 510(k) clearances |
| Jul 18, 2008 | HARVARD MEDICAL DEVICES IR EAR THERMOMETER, MODELS HMIRET-002 AND KINETIK BRANDED IET1 SERIESK081061 · FLL | 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
