ClearanceBrief
510(k) K091681 ยท LRC Instrument, Ent Manual Surgical

FINESS SINUS TREATMENT SYSTEM (ACCESS SHEATH COMPONENT)

ApplicantEntellus Medical, Inc., Maple Grove MN, US
DecisionSubstantially Equivalent, Jul 8, 2009
ReceivedJun 10, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K091681

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.