ClearanceBrief
510(k) K012614 ยท JOW Sleeve, Limb, Compressible

KENDALL, SEQUENTIAL COMPRESSION DEVICE; HUNTLEIGH, FLOWTRON; VENAFLOW; ACUFEX; ALPS; SHEEPSKIN

ApplicantMedical Instruments Technology, Inc., St. George UT, US
DecisionSubstantially Equivalent, May 1, 2002
ReceivedAug 13, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K012614

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.