Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Industrielle Entwicklung Medizintechnik Und Vertri · Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K991545 | WATCH STYLE WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL: KLO | Industrielle Entwicklung Medizintechnik Und Vertri | 2000-01-19 | 261 | 0 |
| K964235 | ABPM MOBIL-O-GRAPH BLOOD PRESSURE MONITOR, MODEL ABP CONTROL | Industrielle Entwicklung Medizintechnik Und Vertri | 1999-03-02 | 860 | 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