Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Rudolf Riester with 33 510(k) clearances. The most recent is a 510(k) clearance dated Jun 24, 2019: Oscillometric Blood Pressure Monitor.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jun 24, 2019 | Oscillometric Blood Pressure MonitorK190927 · DXN | 510(k) clearances |
| Oct 17, 2017 | RVS-100 Vital Signs MonitorK170538 · MWI | 510(k) clearances |
| Oct 4, 2017 | ri-former Predictive ThermometerK171182 · FLL | 510(k) clearances |
| Dec 21, 2000 | EMPIRE N BLOOD PRESSURE MANOMETERSK002955 · DXQ | 510(k) clearances |
| Dec 21, 2000 | RI-SAN/RI-SANA BLOOD PRESSURE MANOMETERSK002954 · DXQ | 510(k) clearances |
| Sep 24, 1997 | SANAPHON NK972378 · DXQ | 510(k) clearances |
| Sep 24, 1997 | PRECISA NK972379 · DXQ | 510(k) clearances |
| Sep 24, 1997 | RI-MEGAK972377 · DXQ | 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
