Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
DQB — Predicate Candidate Screening
3 FDA 510(k) clearances under this product code; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K851102 | VASOSCREEN IMPEDANCE PLETHYSMOGRAPH | Sonicaid, Inc. | 1985-05-16 | 58 | 0 |
| K822873 | DEVETHERM | Eko Scann AB | 1983-03-24 | 178 | 0 |
| K772093 | IMPEDANCE RHEOGRAPH | Dynatech Research & Development Co. | 1977-11-18 | 11 | 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