ClearanceBrief
510(k) K123830 ยท JOW Sleeve, Limb, Compressible

INTERMITTENT PNEUMATIC COMPRESSION DEVICE

ApplicantDalian Labtek Science & Development Co., Ltd., Shanghai, CN
DecisionSubstantially Equivalent, Aug 16, 2013
ReceivedDec 12, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K123830

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.