ClearanceBrief
510(k) K133563 ยท LRC Instrument, Ent Manual Surgical

PATHASSIST LIGHT SEEKER

ApplicantEntellus Medical, Inc., Plymouth MN, US
DecisionSubstantially Equivalent, Dec 20, 2013
ReceivedNov 20, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K133563

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.