510(k) K003038 · OLW Index-Generating Electroencephalograph Software

AGILENT COMPONENT MONITORING SYSTEM, AGILENT V24/26, AGILENT BIS MODULE, MODEL M1175A/76A/77A,REV.L,M1205A,REV.L,M1034A

Applicant	Agilent Technologies Deutschland GmbH, Boeblingen,, DE
Decision	Substantially Equivalent, Dec 15, 2000
Received	Sep 29, 2000
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K003038

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.