ClearanceBrief
510(k) K860256 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

BRAWN AND GROSHONG CATHETERS

ApplicantCatheter Technology Corp., Salt Lake City UT, US
DecisionSubstantially Equivalent, Mar 28, 1986
ReceivedJan 24, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860256

DateFirm and productCodeLinked 510(k)
Oct 1, 2019Bard Peripheral Vascular Inc
1. Groshong 9.5 Dual-Lumen CV Catheter, Ref: 7726950, UDI: (01)00801741041570; 2. Groshong 9.5 F Dual-Lumen CV Catheter, REF: 7726954, UDI: (01)00801741041587
Terminated
LJTNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.