ClearanceBrief
510(k) K173012 ยท JOW Sleeve, Limb, Compressible

ANGIO-PRESS LITE DVT Compression Device

ApplicantPegasus Medical Supply, Inc., Taoyuan County, TW
DecisionSubstantially Equivalent, May 10, 2018
ReceivedSep 27, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K173012

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.