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FDA 510(k)

SERIES 1500 12-LEAD ANALYSIS OPTION

K-Number: K903644 · 1991-12-27

ApplicantMarquette Electronics, Inc.
Decision Date1991-12-27
Product CodeLOS
DecisionSubstantially Equivalent

Device Summary

SERIES 1500 12-LEAD ANALYSIS OPTION 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 1991-12-27 under 510(k) number K903644. The device is classified under product code LOS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERIES 1500 12-LEAD ANALYSIS OPTION?

SERIES 1500 12-LEAD ANALYSIS OPTION is a medical device that received FDA 510(k) clearance on 1991-12-27. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K903644.

When did SERIES 1500 12-LEAD ANALYSIS OPTION receive FDA 510(k) clearance?

SERIES 1500 12-LEAD ANALYSIS OPTION received FDA 510(k) clearance on 1991-12-27, under 510(k) number K903644.

Who is the listed applicant for SERIES 1500 12-LEAD ANALYSIS OPTION?

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 SERIES 1500 12-LEAD ANALYSIS OPTION?

The FDA product code for SERIES 1500 12-LEAD ANALYSIS OPTION is LOS.

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Other records listing Marquette Electronics, Inc. as applicant

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Related Devices (Code: LOS)

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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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