510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K003038Substantially Equivalent

Agilent Component Monitoring System, Agilent V24/26, Agilent Bis Module, Model M1175a/76a/77a,rev.l,m1205a,rev.l,m1034a

Agilent Technologies Deutschland GmbH, Boeblingen,, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K003038 is the FDA 510(k) clearance record for AGILENT COMPONENT MONITORING SYSTEM, AGILENT V24/26, AGILENT BIS MODULE, MODEL M1175A/76A/77A,REV.L,M1205A,REV.L,M1034A, a class II device, cleared for Agilent Technologies Deutschland GmbH on under FDA product code OLW (Index-Generating Electroencephalograph Software). FDA's definition for product code OLW reads: "Analyze electrical activity of the brain by transformation of electroencephalograph signals into a dimensionless index number for use and interpretation by a qualified user". FDA records list 4 510(k) clearances for Agilent Technologies Deutschland GmbH, from to . As of , FDA records show no recalls naming K003038.

Clearance record

Decision date
Received
(77 days to decision)
Product code
OLW Index-Generating Electroencephalograph Software
Regulation
21 CFR 882.1400
Device class
Class II
Review panel
Neurology
Applicant
Agilent Technologies Deutschland GmbH Herrenberger St. 130, Boeblingen,, DE
510(k) summary
Summary
Third party review
No

Clearances, product code OLW

Trailing 12 months
2 clearances under product code OLW in the twelve months to October 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code OLW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20261
September 20260
October 20260