ClearanceBrief
510(k) K102582 ยท JOW Sleeve, Limb, Compressible

ARTERIOFLOW MODEL 7500 SEQUENTIAL COMPRESSION DEVICE

ApplicantDevon Medical, Inc., King Of Prussia PA, US
DecisionSubstantially Equivalent, Oct 7, 2010
ReceivedSep 8, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K102582

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.