ClearanceBrief
510(k) K082025 ยท QPB System, Suction, Lipoplasty For Removal

BODY-JET

ApplicantHuman Med AG, Schwerin, DE
DecisionSubstantially Equivalent, Aug 13, 2008
ReceivedJul 17, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K082025

DateFirm and productCodeLinked 510(k)
Feb 28, 2025HUMAN MED AG
human med Biofill Infiltration Cannula, diameter 2.5mm, 15cm, REF 2024-012, REF 1580107, sterile, single use.
Open, Classified
QPBNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.