ClearanceBrief
510(k) K192802 ยท PND Midline Catheter

primeMidline Catheters

ApplicantPfm Medical, Inc., Carlsbad CA, US
DecisionSubstantially Equivalent, Oct 28, 2019
ReceivedSep 30, 2019
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K192802

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.