Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Imacor, 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) |
|---|---|---|---|---|---|
| K220490 | ImaCor Zura Handheld ZHH-010 | Imacor, Inc. | 2022-04-08 | 45 | 2 |
| K142054 | IMACOR ZURA EVO IMAGING SYSTEM | Imacor, Inc. | 2014-09-29 | 62 | 1 |
| K100989 | ZURA TEE SYSTEM WITH CLARITEE PROBE | Imacor, Inc. | 2010-06-25 | 77 | 1 |
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