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FDA 510(k)

MODEL 78520A ARRHYTHMIA MONITORING SYS

K-Number: K791487 · 1979-08-28

ApplicantHewlett-Packard Co.
Decision Date1979-08-28
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 78520A ARRHYTHMIA MONITORING SYS is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1979-08-28 under 510(k) number K791487. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 78520A ARRHYTHMIA MONITORING SYS?

MODEL 78520A ARRHYTHMIA MONITORING SYS is a medical device that received FDA 510(k) clearance on 1979-08-28. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K791487.

When did MODEL 78520A ARRHYTHMIA MONITORING SYS receive FDA 510(k) clearance?

MODEL 78520A ARRHYTHMIA MONITORING SYS received FDA 510(k) clearance on 1979-08-28, under 510(k) number K791487.

Who is the listed applicant for MODEL 78520A ARRHYTHMIA MONITORING SYS?

The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 78520A ARRHYTHMIA MONITORING SYS?

The FDA product code for MODEL 78520A ARRHYTHMIA MONITORING SYS is DSI.

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Other records listing Hewlett-Packard Co. as applicant

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K992543HEARTSTREAM XLT DEFIBRILLATOR/MONITOR, AC CHARGER, DC CHARGER, DATA CARD, SINGLE BAY ADAPTER, DEFIBRILLATOR PADS CABLEK993587HP M2376A DEVICE LINK SYSTEMK993169MODIFICATION OF: PHYSIOLOGICAL SIGNAL TRANSMITTER AND RECEIVER, MODEL 3810AK992977HEWLETT PACKARD MULTIFUNCTION PEDIATRIC DEFIB FUNCTION, MODEL M3503A & M3504AK993516HP M2600A VIRIDIA TELEMETRY SYSTEMK993171HP VIRIDIA INFORMATION SYSTEM, MODELS M3150A/ M3151A/ M3153A/ M3154A

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Related Devices (Code: DSI)

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.

K243349BodyGuardian Remote Monitoring System (BGRMS v3.0)Boston Scientific Cardiac Diagnostic Technologies, Inc.K250356MoMe ARC® Wireless Ambulatory ECG Monitoring and Detection System (32000)Infobionic, Inc.K240177Zio AT® device (A100A1001)iRhythm Technologies, Inc.K230265MoMe® ARC Wireless Ambulatory ECG Monitoring and Detection SystemInfobionic, Inc.K231276SmartCardia 7L PlatformSmartcardia SAK193104Unified Arrhythmia Diagnostic System PocketECG IVMedicalgorithmics S.A.

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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