Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Midwest Analog & Digital, Inc. · 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) |
|---|---|---|---|---|---|
| K850619 | BEDSIDE PATIENT MONITOR W/MODULES | Midwest Analog & Digital, Inc. | 1985-06-06 | 111 | 0 |
| K781873 | RECORDER, STRIP CHART WITH PRINTER | Midwest Analog & Digital, Inc. | 1979-01-05 | 63 | 0 |
| K780432 | ARRHYTHMIA PROGRAM MODULE | Midwest Analog & Digital, Inc. | 1978-05-26 | 70 | 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