510(k) K830022 · DQO Catheter, Intravascular, Diagnostic

S.M.P. CONTRAST MEDIA SET

Applicant	Omega Technologies, Inc., Mchenry IL, US
Decision	Substantially Equivalent, Jan 21, 1983
Received	Jan 4, 1983
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K830022

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.