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FDA 510(k)

MARQUETTE 1200 DEFIBRILLATION PADS

K-Number: K895651 · 1989-12-12

ApplicantMarquette Electronics, Inc.
Decision Date1989-12-12
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MARQUETTE 1200 DEFIBRILLATION PADS 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 1989-12-12 under 510(k) number K895651. 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 1200 DEFIBRILLATION PADS?

MARQUETTE 1200 DEFIBRILLATION PADS is a medical device that received FDA 510(k) clearance on 1989-12-12. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K895651.

When did MARQUETTE 1200 DEFIBRILLATION PADS receive FDA 510(k) clearance?

MARQUETTE 1200 DEFIBRILLATION PADS received FDA 510(k) clearance on 1989-12-12, under 510(k) number K895651.

Who is the listed applicant for MARQUETTE 1200 DEFIBRILLATION PADS?

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 1200 DEFIBRILLATION PADS?

The FDA product code for MARQUETTE 1200 DEFIBRILLATION PADS 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.

K203231Switched Internal PaddlesPhilips North America, LLCK200849Tempus LS - ManualRemote Diagnostic Technologies, Ltd. A Philips CompanyK182503Sterilizable Internal Defibrillation Paddles for use with LIFEPAK defibrillators/monitorsPhysio-Control, Inc.K103651CARDIOMEDCardio Medical Products, Inc.K103783EURO DEFI PADS ADULT; EURO DEFI PADS ADULT RADIOTRANSPARENT: EURO DEFI PADS PEDIATRICFiab SpaK103334CARDIO MEDCardio Medical Products, 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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