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FDA 510(k)

MUSE-DP

K-Number: K840932 · 1984-10-30

ApplicantMarquette Electronics, Inc.
Decision Date1984-10-30
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MUSE-DP is the device name listed in this FDA 510(k) record. The listed applicant is Marquette Electronics, Inc.. It received FDA 510(k) clearance on 1984-10-30 under 510(k) number K840932. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUSE-DP?

MUSE-DP is a medical device that received FDA 510(k) clearance on 1984-10-30. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K840932.

When did MUSE-DP receive FDA 510(k) clearance?

MUSE-DP received FDA 510(k) clearance on 1984-10-30, under 510(k) number K840932.

Who is the listed applicant for MUSE-DP?

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

What is the FDA product code for MUSE-DP?

The FDA product code for MUSE-DP is DXN.

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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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