Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Artel, Inc. — 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) |
|---|---|---|---|---|---|
| K933836 | HBM HEMOGLOBINOMETER | Artel, Inc. | 1994-03-31 | 238 | 0 |
| K920914 | MP/S SINGLE WAVELENGTH MINI PHOTOMETER | Artel, Inc. | 1992-03-23 | 25 | 0 |
| K914809 | MP MINI PHOTOMETER | Artel, Inc. | 1992-01-27 | 94 | 0 |
| K864542 | ARTEL DIFFERENTIAL PHOTOMETER | Artel, Inc. | 1987-02-06 | 79 | 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