Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Michael S. Upsher · Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K832984 | DISPOSA-LITE LARYNGOSCOPE BLADE | Michael S. Upsher | 1983-10-28 | 56 | 0 |
| K832650 | UPSHER FIBERBRITE LARYNGOSCOPE | Michael S. Upsher | 1983-09-12 | 35 | 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