Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Vesco Medical, LLC · 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) |
|---|---|---|---|---|---|
| K232205 | Vesco Q™ Enteral Feeding Pump; Vesco Q™ 500mL Bag Feed Set; | Vesco Medical, LLC | 2023-10-23 | 90 | 0 |
| K192991 | Vesco Medical Extension Feeding Set | Vesco Medical, LLC | 2020-08-03 | 283 | 0 |
| K170162 | Vesco Medical Nasoenteric Feeding Tubes | Vesco Medical, LLC | 2017-09-26 | 251 | 0 |
| K170218 | Vesco Medical NRFit Tip Syringes | Vesco Medical, LLC | 2017-02-24 | 30 | 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