Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Mediaid, Inc. · 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) |
|---|---|---|---|---|---|
| K071642 | MEDIAID M960 SERIES, VITAL SIGNS MONITOR AND MEDIAID M900 SE | Mediaid, Inc. | 2008-05-02 | 319 | 0 |
| K071610 | MEDIAID PULSE OXIMETER M30 AND M34 | Mediaid, Inc. | 2007-11-05 | 145 | 0 |
| K061896 | MEDIAID DISPOSABLE NON-ADHESIVE SENSORS, MODEL CST050-2101N; | Mediaid, Inc. | 2007-04-12 | 283 | 0 |
| K041964 | MEDIAID REUSABLE FINGER CLIP SPO2 SENSORS AND DISPOSABLE NON | Mediaid, Inc. | 2004-09-14 | 55 | 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