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FDA 510(k)

HIGH RESOLUTION OPTION FOR MAC SERIES ELECTROCARDI

K-Number: K884087 · 1989-02-23

ApplicantMarquette Electronics, Inc.
Decision Date1989-02-23
Product CodeLOS
DecisionSubstantially Equivalent

Device Summary

HIGH RESOLUTION OPTION FOR MAC SERIES ELECTROCARDI 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 1989-02-23 under 510(k) number K884087. The device is classified under product code LOS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIGH RESOLUTION OPTION FOR MAC SERIES ELECTROCARDI?

HIGH RESOLUTION OPTION FOR MAC SERIES ELECTROCARDI is a medical device that received FDA 510(k) clearance on 1989-02-23. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K884087.

When did HIGH RESOLUTION OPTION FOR MAC SERIES ELECTROCARDI receive FDA 510(k) clearance?

HIGH RESOLUTION OPTION FOR MAC SERIES ELECTROCARDI received FDA 510(k) clearance on 1989-02-23, under 510(k) number K884087.

Who is the listed applicant for HIGH RESOLUTION OPTION FOR MAC SERIES ELECTROCARDI?

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 HIGH RESOLUTION OPTION FOR MAC SERIES ELECTROCARDI?

The FDA product code for HIGH RESOLUTION OPTION FOR MAC SERIES ELECTROCARDI is LOS.

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Other records listing Marquette Electronics, 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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