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FDA 510(k)

EAGLE 3000 PATIENT MONITOR

K-Number: K952474 · 1995-10-19

ApplicantMarquette Electronics, Inc.
Decision Date1995-10-19
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EAGLE 3000 PATIENT 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 1995-10-19 under 510(k) number K952474. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EAGLE 3000 PATIENT MONITOR?

EAGLE 3000 PATIENT MONITOR is a medical device that received FDA 510(k) clearance on 1995-10-19. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K952474.

When did EAGLE 3000 PATIENT MONITOR receive FDA 510(k) clearance?

EAGLE 3000 PATIENT MONITOR received FDA 510(k) clearance on 1995-10-19, under 510(k) number K952474.

Who is the listed applicant for EAGLE 3000 PATIENT 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 EAGLE 3000 PATIENT MONITOR?

The FDA product code for EAGLE 3000 PATIENT MONITOR is DRT.

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Related Devices (Code: DRT)

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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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