ClearanceBrief
510(k) K032777 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

MODIFICATION TO: NIPRO SAFE TOUCH SAFETY FISTULA NEEDLE

ApplicantNipro Medical Corp., Weston FL, US
DecisionSubstantially Equivalent, Nov 14, 2003
ReceivedSep 8, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K032777

DateFirm and productCodeLinked 510(k)
Apr 1, 2014Nipro Medical Corporation
NIPRO SafeTouch II Safety AVF Needle, 17G x 1 inch. Item code FS+173230BC.
Terminated
FOZNone listed

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