Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Watermark Medical — 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) |
|---|---|---|---|---|---|
| K160499 | Apnea Risk Evaluation System (ARES), Model 620 | Watermark Medical | 2017-04-24 | 426 | 0 |
| K120325 | CONNECTED CARE MOBILE APPLICATION | Watermark Medical | 2012-07-18 | 167 | 0 |
| K120470 | MIPAL | Watermark Medical | 2012-06-08 | 113 | 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