Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Thermogear, Inc. · 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) |
|---|---|---|---|---|---|
| K083135 | MODIFICATION TO CHILLBUSTER PORTABLE ELECTRIC BLANKET , MODE | Thermogear, Inc. | 2008-10-31 | 8 | 0 |
| K071918 | CHILLBUSTER PORTABLE ELECTRIC BLANKET, MODEL 8002 | Thermogear, Inc. | 2007-11-09 | 120 | 0 |
| K991684 | CHILLBUSTER PORTABLE ELECTRIC BLANKET SYSTEM, MODEL 8001 | Thermogear, Inc. | 2000-03-01 | 289 | 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