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FDA 510(k)

AGILENT INFORMATION CENTER SOFTWARE FOR M3150,M3151,M3153 AND M3154

K-Number: K011093 · 2001-05-01

ApplicantAgilent Technologies, Inc.
Decision Date2001-05-01
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AGILENT INFORMATION CENTER SOFTWARE FOR M3150,M3151,M3153 AND M3154 is the device name listed in this FDA 510(k) record. The listed applicant is Agilent Technologies, Inc.. It received FDA 510(k) clearance on 2001-05-01 under 510(k) number K011093. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AGILENT INFORMATION CENTER SOFTWARE FOR M3150,M3151,M3153 AND M3154?

AGILENT INFORMATION CENTER SOFTWARE FOR M3150,M3151,M3153 AND M3154 is a medical device that received FDA 510(k) clearance on 2001-05-01. The listed applicant is Agilent Technologies, Inc.. The 510(k) number is K011093.

When did AGILENT INFORMATION CENTER SOFTWARE FOR M3150,M3151,M3153 AND M3154 receive FDA 510(k) clearance?

AGILENT INFORMATION CENTER SOFTWARE FOR M3150,M3151,M3153 AND M3154 received FDA 510(k) clearance on 2001-05-01, under 510(k) number K011093.

Who is the listed applicant for AGILENT INFORMATION CENTER SOFTWARE FOR M3150,M3151,M3153 AND M3154?

The FDA 510(k) record lists Agilent Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AGILENT INFORMATION CENTER SOFTWARE FOR M3150,M3151,M3153 AND M3154?

The FDA product code for AGILENT INFORMATION CENTER SOFTWARE FOR M3150,M3151,M3153 AND M3154 is MHX.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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