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FDA 510(k)

LIFEPAK 300 AUTOMATIC ADVISORY DEFIBRILLATOR

K-Number: K902478 · 1990-10-31

ApplicantPhysio-Control Corp.
Decision Date1990-10-31
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIFEPAK 300 AUTOMATIC ADVISORY DEFIBRILLATOR is the device name listed in this FDA 510(k) record. The listed applicant is Physio-Control Corp.. It received FDA 510(k) clearance on 1990-10-31 under 510(k) number K902478. 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 LIFEPAK 300 AUTOMATIC ADVISORY DEFIBRILLATOR?

LIFEPAK 300 AUTOMATIC ADVISORY DEFIBRILLATOR is a medical device that received FDA 510(k) clearance on 1990-10-31. The listed applicant is Physio-Control Corp.. The 510(k) number is K902478.

When did LIFEPAK 300 AUTOMATIC ADVISORY DEFIBRILLATOR receive FDA 510(k) clearance?

LIFEPAK 300 AUTOMATIC ADVISORY DEFIBRILLATOR received FDA 510(k) clearance on 1990-10-31, under 510(k) number K902478.

Who is the listed applicant for LIFEPAK 300 AUTOMATIC ADVISORY DEFIBRILLATOR?

The FDA 510(k) record lists Physio-Control Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIFEPAK 300 AUTOMATIC ADVISORY DEFIBRILLATOR?

The FDA product code for LIFEPAK 300 AUTOMATIC ADVISORY DEFIBRILLATOR is LDD.

Related Clinical Trials

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Other records listing Physio-Control Corp. 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.

K991910LIFEPAK 12 BIPHASICK990338NIBP AND CO2 OPTIONS FOR THE PHYSIO-CONTROL LIFEPAK 12 DEFIBRILLATOR/MONITOR SYSTEMK983393LIFEPAK 500 BIPHASICK973486LIFE PAK 12K962359LIFEPAK 300K955854LIFEPAK 500

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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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