Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Moeller Medical GmbH & Co. KG · Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K072793 | LIPOSAT BASIC (INFILTRATION PUMP), MODEL 92-007 688 | Moeller Medical GmbH & Co. KG | 2008-03-04 | 155 | 0 |
| K053451 | LIPOSAT (INFILTRATION PUMP), MODEL 00 002 274; VACUSAT (SUCT | Moeller Medical GmbH & Co. KG | 2006-08-25 | 256 | 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