ClearanceBrief
510(k) K983050 ยท ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece

PNEUMATIC CUTTER SYSTEM

ApplicantSurgical Laser Technologies, Inc., Montgomeryville PA, US
DecisionSubstantially Equivalent, Nov 25, 1998
ReceivedSep 1, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K983050

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.