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FDA 510(k)

MEDTRONIC PHYSIO-CONTROL LIFEPAK 20 DEFIBRILLATOR/MONITOR/PACEMAKER

K-Number: K012274 · 2002-02-05

ApplicantMedtronic Physio-Control Corp.
Decision Date2002-02-05
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC PHYSIO-CONTROL LIFEPAK 20 DEFIBRILLATOR/MONITOR/PACEMAKER is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Physio-Control Corp.. It received FDA 510(k) clearance on 2002-02-05 under 510(k) number K012274. 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 MEDTRONIC PHYSIO-CONTROL LIFEPAK 20 DEFIBRILLATOR/MONITOR/PACEMAKER?

MEDTRONIC PHYSIO-CONTROL LIFEPAK 20 DEFIBRILLATOR/MONITOR/PACEMAKER is a medical device that received FDA 510(k) clearance on 2002-02-05. The listed applicant is Medtronic Physio-Control Corp.. The 510(k) number is K012274.

When did MEDTRONIC PHYSIO-CONTROL LIFEPAK 20 DEFIBRILLATOR/MONITOR/PACEMAKER receive FDA 510(k) clearance?

MEDTRONIC PHYSIO-CONTROL LIFEPAK 20 DEFIBRILLATOR/MONITOR/PACEMAKER received FDA 510(k) clearance on 2002-02-05, under 510(k) number K012274.

Who is the listed applicant for MEDTRONIC PHYSIO-CONTROL LIFEPAK 20 DEFIBRILLATOR/MONITOR/PACEMAKER?

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

What is the FDA product code for MEDTRONIC PHYSIO-CONTROL LIFEPAK 20 DEFIBRILLATOR/MONITOR/PACEMAKER?

The FDA product code for MEDTRONIC PHYSIO-CONTROL LIFEPAK 20 DEFIBRILLATOR/MONITOR/PACEMAKER is LDD.

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Other records listing Medtronic 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.

K040775LIFEPAK 12K033275LIFEPAK 12, 20, 500, CR PLUSK022732INFANT/CHILD REDUCED ENERGY ELECTRODESK011144LIFEPAK 600 AUTOMATED EXTERNAL DEFIBRILLATORK012428MODIFICATION TO: LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATORK010918LIFEPAK 12 DEFIBRILLATOR/MONITOR SYSTEM

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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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