510(k) K001722 · MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

AGILENT COMPONENT MONITORING SYSTEM; AGILENT INVASIVE BLOOD PRESSURE MODULE

Applicant	Agilent Technologies Deutschland GmbH, Boeblingen,, DE
Decision	Substantially Equivalent, Jun 30, 2000
Received	Jun 6, 2000
Type	Special
FDA record	Open on fda.gov

Recalls that name K001722

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.