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FDA 510(k)

ARRHYTHMIA REVIEW STATION

K-Number: K854136 · 1985-12-04

ApplicantMarquette Electronics, Inc.
Decision Date1985-12-04
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARRHYTHMIA REVIEW STATION 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 1985-12-04 under 510(k) number K854136. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARRHYTHMIA REVIEW STATION?

ARRHYTHMIA REVIEW STATION is a medical device that received FDA 510(k) clearance on 1985-12-04. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K854136.

When did ARRHYTHMIA REVIEW STATION receive FDA 510(k) clearance?

ARRHYTHMIA REVIEW STATION received FDA 510(k) clearance on 1985-12-04, under 510(k) number K854136.

Who is the listed applicant for ARRHYTHMIA REVIEW STATION?

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 ARRHYTHMIA REVIEW STATION?

The FDA product code for ARRHYTHMIA REVIEW STATION is DXG.

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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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