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FDA 510(k)

MARQUETTE EAGLE MONITOR

K-Number: K920790 · 1994-04-19

ApplicantMarquette Electronics, Inc.
Decision Date1994-04-19
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MARQUETTE EAGLE MONITOR 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 1994-04-19 under 510(k) number K920790. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARQUETTE EAGLE MONITOR?

MARQUETTE EAGLE MONITOR is a medical device that received FDA 510(k) clearance on 1994-04-19. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K920790.

When did MARQUETTE EAGLE MONITOR receive FDA 510(k) clearance?

MARQUETTE EAGLE MONITOR received FDA 510(k) clearance on 1994-04-19, under 510(k) number K920790.

Who is the listed applicant for MARQUETTE EAGLE MONITOR?

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 MARQUETTE EAGLE MONITOR?

The FDA product code for MARQUETTE EAGLE MONITOR is DSI.

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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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