Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Intrasense · 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) |
|---|---|---|---|---|---|
| K113620 | MYRIAN 1.11 | Intrasense | 2012-07-12 | 218 | 0 |
| K091001 | MYRIAN 1.4 | Intrasense | 2009-06-29 | 82 | 0 |
| K071000 | MYRIAN | Intrasense | 2007-05-14 | 35 | 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