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FDA 510(k)

SURGICAL MODULE 7000 ECG

K-Number: K840869 · 1985-02-06

ApplicantMarquette Electronics, Inc.
Decision Date1985-02-06
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SURGICAL MODULE 7000 ECG 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 1985-02-06 under 510(k) number K840869. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL MODULE 7000 ECG?

SURGICAL MODULE 7000 ECG is a medical device that received FDA 510(k) clearance on 1985-02-06. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K840869.

When did SURGICAL MODULE 7000 ECG receive FDA 510(k) clearance?

SURGICAL MODULE 7000 ECG received FDA 510(k) clearance on 1985-02-06, under 510(k) number K840869.

Who is the listed applicant for SURGICAL MODULE 7000 ECG?

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 SURGICAL MODULE 7000 ECG?

The FDA product code for SURGICAL MODULE 7000 ECG is DPS.

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Other records listing Marquette Electronics, Inc. as applicant

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Related Devices (Code: DPS)

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.

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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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