Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Avalon Laboratories, LLC — 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) |
|---|---|---|---|---|---|
| K081940 | AVALON ELITE VASCULAR ACCESS KIT | Avalon Laboratories, LLC | 2008-11-18 | 133 | 0 |
| K081820 | AVALON ELITE BI-CAVAL DUAL LUMEN CATHETER, 13FR, 16FR, 19FR, | Avalon Laboratories, LLC | 2008-10-06 | 101 | 0 |
| K081933 | AVALON ELITE MULTI-PORT VENOUS FEMORAL CATHETER, 20FR, 22FR, | Avalon Laboratories, LLC | 2008-10-03 | 88 | 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