ClearanceBrief
510(k) K951684 ยท JOW Sleeve, Limb, Compressible

AIRPERFECT 1000 (SINGLE-USER SYSTEM), AIRPERFECT 2000 (MULTI-USER SYSTEM)

ApplicantDigital Air Corp., Dallas TX, US
DecisionSubstantially Equivalent, Oct 6, 1995
ReceivedApr 11, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K951684

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.