Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Escada International, Inc. · 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) |
|---|---|---|---|---|---|
| K080102 | TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIAN | Escada International, Inc. | 2008-08-20 | 219 | 0 |
| K071445 | TERRAQUANT MQ2000 V.5 WITH THE TQ-1TENS | Escada International, Inc. | 2007-10-29 | 158 | 0 |
| K061614 | TERRAQUANT MQ2000 V. 5 AND HANDYRX MQ2007 LASERS | Escada International, Inc. | 2006-10-06 | 119 | 0 |
| K043055 | TERRAQUANT MQ2000 LASER THERAPY DEVICE | Escada International, Inc. | 2005-07-25 | 262 | 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