510(k) K864007 · DXE Catheter, Embolectomy

EMBOLECTOMY/THROMBECTOMY BALLOON CATHETER

Applicant	Uresil Corp., Skokie IL, US
Decision	Substantially Equivalent, Jan 2, 1987
Received	Oct 15, 1986
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K864007

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.