Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
NYV — Predicate Candidate Screening
5 FDA 510(k) clearances under this product code; the 50 most recent screened below.
90 daysmedian FDA review time
210 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K253569 | Atmo Gas Capsule System | Atmo Biosciences, Ltd. | 2026-05-22 | 186 | 0 |
| K250940 | Atmo Gas Capsule System | Atmo Biosciences, Ltd. | 2025-06-26 | 90 | 0 |
| K250493 | MotiliCap GI Monitoring System | Anx Robotica Corporation | 2025-05-21 | 90 | 0 |
| K092342 | SMARTPILL GI MONITORING SYSTEM, VERSION 2.0 | The Smartpill Corporation | 2009-10-30 | 87 | 0 |
| K053547 | SMARTPILL GI MONITORING SYSTEM | The Smartpill Corporation | 2006-07-18 | 210 | 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