Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Alcide Corp. — Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K952929 | LD GENERAL PURPOSE DISINFECTANT | Alcide Corp. | 1995-10-07 | 110 | 0 |
| K953241 | EXSPOR | Alcide Corp. | 1995-09-29 | 80 | 0 |
| K853413 | RENNEW-D SPORICIDE/DISINFECTANT FOR HEMODIALYZERS | Alcide Corp. | 1985-09-06 | 23 | 0 |
| K844734 | ALCIDE REN NEW-D | Alcide Corp. | 1985-05-17 | 164 | 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