ClearanceBrief
510(k) K840342 ยท FRG Wrap, Sterilization

PDI PREPMASTER WET PACK PATIENT PREP KIT

ApplicantNice-Pak Products, Inc., Walker MI, US
DecisionSubstantially Equivalent, Mar 27, 1984
ReceivedJan 6, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K840342

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.