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FDA 510(k)

MARQUETTE SV O2 MODULE

K-Number: K915073 · 1992-12-29

Decision Date1992-12-29
Product CodeDQE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MARQUETTE SV O2 MODULE 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 1992-12-29 under 510(k) number K915073. The device is classified under product code DQE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARQUETTE SV O2 MODULE?

MARQUETTE SV O2 MODULE is a medical device that received FDA 510(k) clearance on 1992-12-29. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K915073.

When did MARQUETTE SV O2 MODULE receive FDA 510(k) clearance?

MARQUETTE SV O2 MODULE received FDA 510(k) clearance on 1992-12-29, under 510(k) number K915073.

Who is the listed applicant for MARQUETTE SV O2 MODULE?

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 MARQUETTE SV O2 MODULE?

The FDA product code for MARQUETTE SV O2 MODULE is DQE.

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.

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Related Devices (Code: DQE)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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