Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Mimvista 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) |
|---|---|---|---|---|---|
| K071964 | MIM 4.1 (SEASTAR) | Mimvista Corp. | 2007-09-26 | 72 | 2 |
| K062163 | MIMVIEWER | Mimvista Corp. | 2006-09-22 | 56 | 0 |
| K060816 | MIM 4.0 (NEURO | Mimvista Corp. | 2006-05-16 | 50 | 1 |
| K052379 | MIM 3.5 (CIRCA) | Mimvista Corp. | 2005-10-31 | 62 | 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