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FDA 510(k)

THREE CHANNEL MONITOR SERIES 6700

K-Number: K830899 · 1983-04-12

Decision Date1983-04-12
Product CodeDXJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

THREE CHANNEL MONITOR SERIES 6700 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 1983-04-12 under 510(k) number K830899. The device is classified under product code DXJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THREE CHANNEL MONITOR SERIES 6700?

THREE CHANNEL MONITOR SERIES 6700 is a medical device that received FDA 510(k) clearance on 1983-04-12. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K830899.

When did THREE CHANNEL MONITOR SERIES 6700 receive FDA 510(k) clearance?

THREE CHANNEL MONITOR SERIES 6700 received FDA 510(k) clearance on 1983-04-12, under 510(k) number K830899.

Who is the listed applicant for THREE CHANNEL MONITOR SERIES 6700?

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 THREE CHANNEL MONITOR SERIES 6700?

The FDA product code for THREE CHANNEL MONITOR SERIES 6700 is DXJ.

Related Clinical Trials

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.

Other records listing Marquette Electronics, Inc. as applicant

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.

View all 82 devices →

Related Devices (Code: DXJ)

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.

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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