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FDA 510(k)

VPD-261 DEFIBRILLATOR MONITOR

K-Number: K822294 · 1982-08-31

ApplicantLife Science Instrumentation, Inc.
Decision Date1982-08-31
Product CodeLDD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VPD-261 DEFIBRILLATOR MONITOR 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 1982-08-31 under 510(k) number K822294. 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 VPD-261 DEFIBRILLATOR MONITOR?

VPD-261 DEFIBRILLATOR MONITOR is a medical device that received FDA 510(k) clearance on 1982-08-31. The listed applicant is Life Science Instrumentation, Inc.. The 510(k) number is K822294.

When did VPD-261 DEFIBRILLATOR MONITOR receive FDA 510(k) clearance?

VPD-261 DEFIBRILLATOR MONITOR received FDA 510(k) clearance on 1982-08-31, under 510(k) number K822294.

Who is the listed applicant for VPD-261 DEFIBRILLATOR MONITOR?

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 VPD-261 DEFIBRILLATOR MONITOR?

The FDA product code for VPD-261 DEFIBRILLATOR MONITOR 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 5K843396LS-260G MONITOR/RECORDER & DEFIBILLATORK840246MINI-DEFIBRILLATOR 280/4K831056DEFIBRILLATOR VPD 545K822617VPD540 DEFIBRILLATOR

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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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