Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Medwaves Incorporated — 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) |
|---|---|---|---|---|---|
| K143203 | AveCure Microwave Coagulation-Ablation Generator, AveCure Mi | Medwaves Incorporated | 2015-08-26 | 292 | 0 |
| K083537 | MODIFICATION TO MEDWAVES MICROWAVE COAGULATION/ABLATION SYST | Medwaves Incorporated | 2009-01-15 | 48 | 0 |
| K070356 | MEDWAVES MICROWAVE COAGULATION/ABLATION SYSTEM | Medwaves Incorporated | 2007-12-18 | 315 | 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