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FDA 510(k)

MODIFICATION TO DEVICE LINK SYSTEM, MODEL M2376A

K-Number: K012094 · 2001-07-20

ApplicantAgilent Technologies, Inc.
Decision Date2001-07-20
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO DEVICE LINK SYSTEM, MODEL M2376A 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 2001-07-20 under 510(k) number K012094. 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 MODIFICATION TO DEVICE LINK SYSTEM, MODEL M2376A?

MODIFICATION TO DEVICE LINK SYSTEM, MODEL M2376A is a medical device that received FDA 510(k) clearance on 2001-07-20. The listed applicant is Agilent Technologies, Inc.. The 510(k) number is K012094.

When did MODIFICATION TO DEVICE LINK SYSTEM, MODEL M2376A receive FDA 510(k) clearance?

MODIFICATION TO DEVICE LINK SYSTEM, MODEL M2376A received FDA 510(k) clearance on 2001-07-20, under 510(k) number K012094.

Who is the listed applicant for MODIFICATION TO DEVICE LINK SYSTEM, MODEL M2376A?

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 MODIFICATION TO DEVICE LINK SYSTEM, MODEL M2376A?

The FDA product code for MODIFICATION TO DEVICE LINK SYSTEM, MODEL M2376A 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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