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FDA 510(k)

ADULT MONITORING ELECTOR@@RODE 9431-300

K-Number: K833695 · 1984-01-27

ApplicantMarquette Electronics, Inc.
Decision Date1984-01-27
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ADULT MONITORING ELECTOR@@RODE 9431-300 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 1984-01-27 under 510(k) number K833695. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADULT MONITORING ELECTOR@@RODE 9431-300?

ADULT MONITORING ELECTOR@@RODE 9431-300 is a medical device that received FDA 510(k) clearance on 1984-01-27. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K833695.

When did ADULT MONITORING ELECTOR@@RODE 9431-300 receive FDA 510(k) clearance?

ADULT MONITORING ELECTOR@@RODE 9431-300 received FDA 510(k) clearance on 1984-01-27, under 510(k) number K833695.

Who is the listed applicant for ADULT MONITORING ELECTOR@@RODE 9431-300?

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 ADULT MONITORING ELECTOR@@RODE 9431-300?

The FDA product code for ADULT MONITORING ELECTOR@@RODE 9431-300 is DRX.

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Other records listing Marquette Electronics, Inc. as applicant

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Related Devices (Code: DRX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K171244PhysiotraceNimbleheart, Inc.K123658BIOMODULE 3-M1Zephyr Technology CorporationK101576CENTERRIDGE DIAGNOSTIC ECG ELECTRODE, CENTERRIDGE MONITORING ECG ELECTRODESTeam Innovations, Inc.K101685IP-SETIntegral Process SasK100129AMBU BLUE SENSOR NEO, AMBU BLUE SENSOR NEO XAmbu A/SK093327INTCO TAB ELECTRODEShanghai Intco Electrode Manufacturing Co., Ltd.

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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