Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
D&K Stores, 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) |
|---|---|---|---|---|---|
| K970101 | JAMES ALEX SUNGLASSES | D&K Stores, Inc. | 1997-03-04 | 50 | 0 |
| K960798 | D & K SUNGLASSES | D&K Stores, Inc. | 1996-04-24 | 57 | 0 |
| K960797 | D & K SUNGLASSES | D&K Stores, Inc. | 1996-03-12 | 14 | 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