Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Sunbeam Corp. · 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) |
|---|---|---|---|---|---|
| K842275 | ULTRASONIC COOL SPRAY HUMIDIFIER | Sunbeam Corp. | 1984-08-14 | 67 | 0 |
| K801776 | COLD PACK #589 | Sunbeam Corp. | 1980-08-07 | 10 | 0 |
| K780360 | MASSAGER, GUM/SSAGE POWERED GUM | Sunbeam Corp. | 1978-05-26 | 81 | 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