Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
CHG · 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) |
|---|---|---|---|---|---|
| K941807 | INTERSECT SYSTEMS' NON-MERCURIC CHLORIDE REAGENT | Intersect Systems, Inc. | 1994-09-14 | 155 | 0 |
| K934588 | CHLORIDE (MF) ASSAY | Diagnostic Chemicals , Ltd. | 1994-02-18 | 148 | 0 |
| K903103 | SYNERMED CHLORIDE REAGENT KIT | Synermed, Inc. | 1990-08-09 | 27 | 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