Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
GIG · 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) |
|---|---|---|---|---|---|
| K973995 | RANDOX BILIRUBIN | Randox Laboratories, Ltd. | 1997-12-08 | 48 | 0 |
| K933836 | HBM HEMOGLOBINOMETER | Artel, Inc. | 1994-03-31 | 238 | 0 |
| K771101 | HEMOGLOBIN ANALYZER & PERFORM. CHECK SET | The Dow Chemical Co. | 1977-07-21 | 31 | 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