ClearanceBrief
510(k) K183328 ยท JOW Sleeve, Limb, Compressible

Pulse Rx 2.0, Pulse Pro Rx 2.0

ApplicantNormaTec Industries, LP, Watertown MA, US
DecisionSubstantially Equivalent, Dec 21, 2018
ReceivedNov 30, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K183328

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.