510(k) K002030 · MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

OMNI-TRAK 3150/3155A SERIES MONITOR WITH ANESTHETIC AGENT, MODEL 3155A SERIES

Applicant	Invivo Research, Inc., Orlando FL, US
Decision	Substantially Equivalent, Sep 26, 2000
Received	Jul 3, 2000
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K002030

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.