Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
PID · Predicate Candidate Screening
3 FDA 510(k) clearances under this product code; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K182895 | Wilson-Cook Achalasia Balloon | Wilson-Cook Medical, Inc. | 2019-01-25 | 102 | 0 |
| K132337 | ESOFLIP BALLOON DILATION CATHETER | Crospon, Ltd. | 2013-10-07 | 73 | 1 |
| K050232 | RIGIFLEX SINGLE-USE ACHALASIA BALLOON DILATOR | Boston Scientific Corp | 2005-03-11 | 38 | 1 |
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