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FDA 510(k)

QT DISPERSION AND T WAVE ANALYSIS PROGRAM (QT GUARD ANALYSIS SYSTEM)

K-Number: K981024 · 1998-10-06

ApplicantMarquette Medical Systems, Inc.
Decision Date1998-10-06
Product CodeLOS
DecisionSubstantially Equivalent

Device Summary

QT DISPERSION AND T WAVE ANALYSIS PROGRAM (QT GUARD ANALYSIS SYSTEM) is the device name listed in this FDA 510(k) record. The listed applicant is Marquette Medical Systems, Inc.. It received FDA 510(k) clearance on 1998-10-06 under 510(k) number K981024. The device is classified under product code LOS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QT DISPERSION AND T WAVE ANALYSIS PROGRAM (QT GUARD ANALYSIS SYSTEM)?

QT DISPERSION AND T WAVE ANALYSIS PROGRAM (QT GUARD ANALYSIS SYSTEM) is a medical device that received FDA 510(k) clearance on 1998-10-06. The listed applicant is Marquette Medical Systems, Inc.. The 510(k) number is K981024.

When did QT DISPERSION AND T WAVE ANALYSIS PROGRAM (QT GUARD ANALYSIS SYSTEM) receive FDA 510(k) clearance?

QT DISPERSION AND T WAVE ANALYSIS PROGRAM (QT GUARD ANALYSIS SYSTEM) received FDA 510(k) clearance on 1998-10-06, under 510(k) number K981024.

Who is the listed applicant for QT DISPERSION AND T WAVE ANALYSIS PROGRAM (QT GUARD ANALYSIS SYSTEM)?

The FDA 510(k) record lists Marquette Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for QT DISPERSION AND T WAVE ANALYSIS PROGRAM (QT GUARD ANALYSIS SYSTEM)?

The FDA product code for QT DISPERSION AND T WAVE ANALYSIS PROGRAM (QT GUARD ANALYSIS SYSTEM) is LOS.

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Other records listing Marquette Medical Systems, Inc. as applicant

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Related Devices (Code: LOS)

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.

K090895EKG-PLUS II SOFTWAREBionet Co., Ltd.K083749CARDIOVIEW32 REVIEW MODULEQrs Diagnostic, LLCK073376PHILIPS ECG ALGORITHMPhilips Medical SystemsK023034CARDIOTOUCH-3000Bionet Company, Ltd.K011328CARDIO CARE EKG-2000 12-CHANNEL ELECTROCARDIOGRAPHBionet Company, Ltd.K993616CARDIO-CARD INTERPRETATION SYSTEM INasiff Assoc., Inc.

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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