ClearanceBrief
510(k) K172779 ยท JOW Sleeve, Limb, Compressible

AIROS 8 Sequential Compression Device

ApplicantAiros Medical, Inc., Audubon PA, US
DecisionSubstantially Equivalent, Jun 22, 2018
ReceivedSep 14, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K172779

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.