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FDA 510(k)

SERVOMED ARRHYCOMP CENTRAL MONITOR SYS

K-Number: K840899 · 1984-11-20

ApplicantLitton Medical Electronics
Decision Date1984-11-20
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SERVOMED ARRHYCOMP CENTRAL MONITOR SYS is the device name listed in this FDA 510(k) record. The listed applicant is Litton Medical Electronics. It received FDA 510(k) clearance on 1984-11-20 under 510(k) number K840899. 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 SERVOMED ARRHYCOMP CENTRAL MONITOR SYS?

SERVOMED ARRHYCOMP CENTRAL MONITOR SYS is a medical device that received FDA 510(k) clearance on 1984-11-20. The listed applicant is Litton Medical Electronics. The 510(k) number is K840899.

When did SERVOMED ARRHYCOMP CENTRAL MONITOR SYS receive FDA 510(k) clearance?

SERVOMED ARRHYCOMP CENTRAL MONITOR SYS received FDA 510(k) clearance on 1984-11-20, under 510(k) number K840899.

Who is the listed applicant for SERVOMED ARRHYCOMP CENTRAL MONITOR SYS?

The FDA 510(k) record lists Litton Medical Electronics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SERVOMED ARRHYCOMP CENTRAL MONITOR SYS?

The FDA product code for SERVOMED ARRHYCOMP CENTRAL MONITOR SYS is DSI.

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Other records listing Litton Medical Electronics 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.

K840522RECOMED BLOOD-FLOW METER H236-052-02K840439RECOMED CARDIAC OUTPUT METER 236067-K840523SERVOMED PULSE AMPLIFIER MODULE-206-K840524SERVOMED BASIC BEDSIDE UNIT SMV 110TPK840209SERVOMED MEDIVISION SCOPE SMV-235K840832SERVOMED OXCARDIORE SPIROGRAPH 324/111

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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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