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FDA 510(k)

MARQUETTE SERIES 360 DEFIBRILLATOR

K-Number: K921487 · 1992-12-29

ApplicantMarquette Electronics, Inc.
Decision Date1992-12-29
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MARQUETTE SERIES 360 DEFIBRILLATOR 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 K921487. The device is classified under product code LDD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARQUETTE SERIES 360 DEFIBRILLATOR?

MARQUETTE SERIES 360 DEFIBRILLATOR 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 K921487.

When did MARQUETTE SERIES 360 DEFIBRILLATOR receive FDA 510(k) clearance?

MARQUETTE SERIES 360 DEFIBRILLATOR received FDA 510(k) clearance on 1992-12-29, under 510(k) number K921487.

Who is the listed applicant for MARQUETTE SERIES 360 DEFIBRILLATOR?

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 SERIES 360 DEFIBRILLATOR?

The FDA product code for MARQUETTE SERIES 360 DEFIBRILLATOR is LDD.

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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.

K971868IMPACT (INFORMING MOBILE PERSONNEL AND CARE TRACKING) PAGER SYSTEMK971683WIRELESS LAN (LOCAL AREA NETWORK) - WIRELESS ETHERNETK972199SIGNAL-AVERAGED HIGH RESOLUTION P WAVE ANALYSISK962547CARDIOSERV PK963120RESPONDER 2500 DEFIBRILLATOR AND CARDIAC CARE SYSTEMK962827ALARM DISPLAY UNIT/PAGER-LAN SYSTEM (ADU)

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Related Devices (Code: LDD)

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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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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