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FDA 510(k)

LS-260G MONITOR/RECORDER & DEFIBILLATOR

K-Number: K843396 · 1984-10-19

ApplicantLife Science Instrumentation, Inc.
Decision Date1984-10-19
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LS-260G MONITOR/RECORDER & DEFIBILLATOR is the device name listed in this FDA 510(k) record. The listed applicant is Life Science Instrumentation, Inc.. It received FDA 510(k) clearance on 1984-10-19 under 510(k) number K843396. 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 LS-260G MONITOR/RECORDER & DEFIBILLATOR?

LS-260G MONITOR/RECORDER & DEFIBILLATOR is a medical device that received FDA 510(k) clearance on 1984-10-19. The listed applicant is Life Science Instrumentation, Inc.. The 510(k) number is K843396.

When did LS-260G MONITOR/RECORDER & DEFIBILLATOR receive FDA 510(k) clearance?

LS-260G MONITOR/RECORDER & DEFIBILLATOR received FDA 510(k) clearance on 1984-10-19, under 510(k) number K843396.

Who is the listed applicant for LS-260G MONITOR/RECORDER & DEFIBILLATOR?

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

What is the FDA product code for LS-260G MONITOR/RECORDER & DEFIBILLATOR?

The FDA product code for LS-260G MONITOR/RECORDER & DEFIBILLATOR is LDD.

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Other records listing Life Science Instrumentation, 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.

K850812EMERGIPACE - EXTERNAL PACEMAKERK842037LS 5K840246MINI-DEFIBRILLATOR 280/4K831056DEFIBRILLATOR VPD 545K822617VPD540 DEFIBRILLATORK822616LS6 ARRYTHMIA DISCRIMINATOR

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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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