ClearanceBrief
510(k) K931327 ยท DQX Wire, Guide, Catheter

PSG DIRECTIONAL HYDROPHILIC GUIDE WIRE

ApplicantPeripheral Systems Group, Mountain View CA, US
DecisionSubstantially Equivalent, Jul 14, 1993
ReceivedMar 16, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K931327

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.