510(k) K883768 · LFJ Catheter, Subclavian

VAS-CATH CATHETER REPAIR KIT

Applicant	Vas-Cath, Inc., Mississauga, Ontario, CA
Decision	Substantially Equivalent, Nov 14, 1988
Received	Sep 6, 1988
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K883768

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.