510(k) K083325 · DQA Oximeter

N-600X WITH SPD, OXIMAX N-600X

Applicant	Covidien, Boulder CO, US
Decision	Substantially Equivalent, Mar 9, 2009
Received	Nov 12, 2008
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K083325

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.