Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Amira Medical, Inc. · 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) |
|---|---|---|---|---|---|
| K010605 | ATLAST DATA MANAGEMENT SOFTWARE (DMS) | Amira Medical, Inc. | 2001-05-07 | 68 | 0 |
| K991075 | ATLAST GLUCOSE CONTROL SOLUTION | Amira Medical, Inc. | 1999-05-10 | 40 | 0 |
| K982076 | AMIRA MEDICAL ATLAST BLOOD GLUCOSE MONITORING SYSTEM | Amira Medical, Inc. | 1998-12-10 | 181 | 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