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FDA 510(k)

LIFE DEFENSE PLUS(TM), DEFIBRILLATOR/MONITOR/PACER

K-Number: K895533 · 1990-01-26

ApplicantMatrix Medica, Inc.
Decision Date1990-01-26
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIFE DEFENSE PLUS(TM), DEFIBRILLATOR/MONITOR/PACER is the device name listed in this FDA 510(k) record. The listed applicant is Matrix Medica, Inc.. It received FDA 510(k) clearance on 1990-01-26 under 510(k) number K895533. 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 LIFE DEFENSE PLUS(TM), DEFIBRILLATOR/MONITOR/PACER?

LIFE DEFENSE PLUS(TM), DEFIBRILLATOR/MONITOR/PACER is a medical device that received FDA 510(k) clearance on 1990-01-26. The listed applicant is Matrix Medica, Inc.. The 510(k) number is K895533.

When did LIFE DEFENSE PLUS(TM), DEFIBRILLATOR/MONITOR/PACER receive FDA 510(k) clearance?

LIFE DEFENSE PLUS(TM), DEFIBRILLATOR/MONITOR/PACER received FDA 510(k) clearance on 1990-01-26, under 510(k) number K895533.

Who is the listed applicant for LIFE DEFENSE PLUS(TM), DEFIBRILLATOR/MONITOR/PACER?

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

What is the FDA product code for LIFE DEFENSE PLUS(TM), DEFIBRILLATOR/MONITOR/PACER?

The FDA product code for LIFE DEFENSE PLUS(TM), DEFIBRILLATOR/MONITOR/PACER is LDD.

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Other records listing Matrix Medica, 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.

K961536FLEXSCOPEK923693KLORMANK921982MATRX HOPE(R) 5 RESUSCITATORK915353MATRX MEDICAL MAXIMIZER 1000 AND 2000 VACUUM PUMPK912661MATRX, PYRAMID TRIANGLE BANDAGEK900551MATRX DISPOSABLE NON-INVASIVE GELLED PACING ELEC.

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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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