Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Pace Tech Medical Monitors, 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) |
|---|---|---|---|---|---|
| K970445 | VITALMAX 4000 CONFIGURED/VITALMAX 4000 MODULAR/VITALMAX 4100 | Pace Tech Medical Monitors, Inc. | 1998-01-30 | 359 | 0 |
| K932203 | VITALMAX 530 | Pace Tech Medical Monitors, Inc. | 1994-07-19 | 439 | 0 |
| K914164 | VITALMAX 840 SERIES | Pace Tech Medical Monitors, Inc. | 1993-04-09 | 570 | 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