Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Moller Medical GmbH · Predicate Candidate Screening

3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K162588Möller Medical Biopsy Needles and SystemsMoller Medical GmbH2017-06-192760
K150898LiquoGuard 7, LiquoGuard 7 Drainage Set, Lenght 2000mmMoller Medical GmbH2015-12-182600
K121248LIQUOGUARD CSF LIQUOGUARD CSF TUBING SET (1500MM) LIQUOGUARDMoller Medical GmbH2013-12-135970

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