Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
The Rupp & Bowman Co. — Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K880973 | MICROLYTE 7 | The Rupp & Bowman Co. | 1988-09-07 | 183 | 0 |
| K882081 | SPECIFIC CHEMISTRY ANALYZER | The Rupp & Bowman Co. | 1988-07-01 | 45 | 0 |
| K880242 | KONE CALCIUM TEST | The Rupp & Bowman Co. | 1988-03-15 | 55 | 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