ClearanceBrief
510(k) K032690 ยท LFL Instrument, Ultrasonic Surgical

MISONIX INC. FS 1000 RF ULTRASONIC SURGICAL ASPIRATOR SYSTEM

ApplicantMisonix, Inc., Farmingdale NY, US
DecisionSubstantially Equivalent, Dec 9, 2003
ReceivedSep 2, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K032690

No recall in the FDA data names this 510(k).

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