Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Agilent Technologies Deutschland GmbH · 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) |
|---|---|---|---|---|---|
| K002758 | AGILENT COMPONENT MONITORING SYSTEM, AGILENT CARDIAC OUTPUT | Agilent Technologies Deutschland GmbH | 2001-02-22 | 170 | 0 |
| K003038 | AGILENT COMPONENT MONITORING SYSTEM, AGILENT V24/26, AGILENT | Agilent Technologies Deutschland GmbH | 2000-12-15 | 77 | 0 |
| K001722 | AGILENT COMPONENT MONITORING SYSTEM; AGILENT INVASIVE BLOOD | Agilent Technologies Deutschland GmbH | 2000-06-30 | 24 | 0 |
| K001333 | AGILENT COMPONENT MONITORING SYSTEM, AGILENT MULTI-MEASUREME | Agilent Technologies Deutschland GmbH | 2000-05-17 | 20 | 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