ClearanceBrief
510(k) K990366 ยท LRC Instrument, Ent Manual Surgical

EXMOOR SUCTION CLEARANCE KIT

ApplicantExmoor Plastics , Ltd., Taunton, GB
DecisionSubstantially Equivalent, Mar 5, 1999
ReceivedFeb 5, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K990366

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.