Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Rahn Laboratories — 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) |
|---|---|---|---|---|---|
| K900266 | STERILE CARBON STEEL SURGICAL BLADE | Rahn Laboratories | 1990-03-01 | 42 | 0 |
| K892461 | NON-STERILE LATEX EXAMINATION GLOVES | Rahn Laboratories | 1989-07-28 | 112 | 0 |
| K881479 | OPERATION ROOM TOWEL | Rahn Laboratories | 1988-04-14 | 7 | 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