ClearanceBrief
510(k) K083060 ยท NLQ Single-Use Reprocessed Ultrasonic Surgical Instruments

REPROCESSED HARMONIC SCALPEL

ApplicantSterilmed, Inc., Maple Grove MN, US
DecisionSubstantially Equivalent, Jan 9, 2009
ReceivedOct 14, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K083060

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.