Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Rud Riester GmbH & CO KG · Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K944337 | VARIOUS STETHOSCOPES | Rud Riester GmbH & CO KG | 1994-11-30 | 85 | 0 |
| K942649 | MINIMUS I; MINIMUS III, SANAPHON | Rud Riester GmbH & CO KG | 1994-11-29 | 182 | 0 |
| K942650 | BIG BEN | Rud Riester GmbH & CO KG | 1994-08-15 | 76 | 0 |
| K943461 | VARIOUS TYPES OF MERCURIALS | Rud Riester GmbH & CO KG | 1994-07-27 | 9 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda