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FDA 510(k)

M2376A DEVICELINK SYSTEM

K-Number: K003107 · 2000-10-19

ApplicantAgilent Technologies, Inc.
Decision Date2000-10-19
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

M2376A DEVICELINK SYSTEM 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 2000-10-19 under 510(k) number K003107. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the M2376A DEVICELINK SYSTEM?

M2376A DEVICELINK SYSTEM is a medical device that received FDA 510(k) clearance on 2000-10-19. The listed applicant is Agilent Technologies, Inc.. The 510(k) number is K003107.

When did M2376A DEVICELINK SYSTEM receive FDA 510(k) clearance?

M2376A DEVICELINK SYSTEM received FDA 510(k) clearance on 2000-10-19, under 510(k) number K003107.

Who is the listed applicant for M2376A DEVICELINK SYSTEM?

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 M2376A DEVICELINK SYSTEM?

The FDA product code for M2376A DEVICELINK SYSTEM is MWI.

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Related Devices (Code: MWI)

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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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