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FDA 510(k)

CD TELEMETRY SYSTEMS

K-Number: K891104 · 1989-04-19

Decision Date1989-04-19
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CD TELEMETRY SYSTEMS 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 1989-04-19 under 510(k) number K891104. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CD TELEMETRY SYSTEMS?

CD TELEMETRY SYSTEMS is a medical device that received FDA 510(k) clearance on 1989-04-19. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K891104.

When did CD TELEMETRY SYSTEMS receive FDA 510(k) clearance?

CD TELEMETRY SYSTEMS received FDA 510(k) clearance on 1989-04-19, under 510(k) number K891104.

Who is the listed applicant for CD TELEMETRY SYSTEMS?

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 CD TELEMETRY SYSTEMS?

The FDA product code for CD TELEMETRY SYSTEMS is DRG.

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: DRG)

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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