Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
HJE · 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) |
|---|---|---|---|---|---|
| K922348 | VALTRAC(R) INTRODUCER FORCEP | American Cyanamid Co. | 1992-06-09 | 21 | 0 |
| K802291 | FLUORESCENT SUN LAMP FIXTURE | Strato-Ray Co. | 1980-10-31 | 42 | 0 |
| K781698 | EXAMINER 10 | American Sterilizer Co. | 1978-11-03 | 24 | 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