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 D. E. Hokanson, Inc. with 19 510(k) clearances. The most recent is a 510(k) clearance dated Aug 6, 2004: POLYURETHANE BLOOD PRESSURE CUFFS.
| Aug 6, 2004 | POLYURETHANE BLOOD PRESSURE CUFFSK041689 · DXQ | 510(k) clearances |
| Dec 9, 2003 | OB1 OBSTETRICAL DOPPLERK033156 · KNG | 510(k) clearances |
| Feb 12, 2003 | A16 BLOOD FLOW MEASUREMENT SYSTEMK023707 · JOM | 510(k) clearances |
| Aug 26, 1998 | EC6 PLETHYSMOGRAPHK982707 · JOM | 510(k) clearances |
| Aug 12, 1998 | ANS 2000 ECG MONITOR AND RESPIRATION PACERK973426 · DPS | 510(k) clearances |
| Oct 3, 1997 | NIVP3 (WINDOWS VERSION OF NIVPK970570 · DQK | 510(k) clearances |
| Feb 4, 1994 | NON INVASIVE VASCULAR PROGRAMK932852 · JOB | 510(k) clearances |
| Jan 13, 1994 | EC 5R PLETHYSMOGRAPHK932812 · JEH | 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
