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FDA 510(k)

CENTRAL STATION DISPLAY/RECORDER MATRIX

K-Number: K830517 · 1983-06-15

ApplicantMarquette Electronics, Inc.
Decision Date1983-06-15
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CENTRAL STATION DISPLAY/RECORDER MATRIX 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 1983-06-15 under 510(k) number K830517. 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 CENTRAL STATION DISPLAY/RECORDER MATRIX?

CENTRAL STATION DISPLAY/RECORDER MATRIX is a medical device that received FDA 510(k) clearance on 1983-06-15. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K830517.

When did CENTRAL STATION DISPLAY/RECORDER MATRIX receive FDA 510(k) clearance?

CENTRAL STATION DISPLAY/RECORDER MATRIX received FDA 510(k) clearance on 1983-06-15, under 510(k) number K830517.

Who is the listed applicant for CENTRAL STATION DISPLAY/RECORDER MATRIX?

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 CENTRAL STATION DISPLAY/RECORDER MATRIX?

The FDA product code for CENTRAL STATION DISPLAY/RECORDER MATRIX is DRT.

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Other records listing Marquette Electronics, Inc. as applicant

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Related Devices (Code: DRT)

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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