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FDA 510(k)

SERVOMED BASIC BEDSIDE UNIT SMV 107

K-Number: K831782 · 1983-11-16

ApplicantLitton Medical Electronics
Decision Date1983-11-16
Product CodeDXJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SERVOMED BASIC BEDSIDE UNIT SMV 107 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 1983-11-16 under 510(k) number K831782. The device is classified under product code DXJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERVOMED BASIC BEDSIDE UNIT SMV 107?

SERVOMED BASIC BEDSIDE UNIT SMV 107 is a medical device that received FDA 510(k) clearance on 1983-11-16. The listed applicant is Litton Medical Electronics. The 510(k) number is K831782.

When did SERVOMED BASIC BEDSIDE UNIT SMV 107 receive FDA 510(k) clearance?

SERVOMED BASIC BEDSIDE UNIT SMV 107 received FDA 510(k) clearance on 1983-11-16, under 510(k) number K831782.

Who is the listed applicant for SERVOMED BASIC BEDSIDE UNIT SMV 107?

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 BASIC BEDSIDE UNIT SMV 107?

The FDA product code for SERVOMED BASIC BEDSIDE UNIT SMV 107 is DXJ.

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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 H236-052-02K840899SERVOMED ARRHYCOMP CENTRAL MONITOR SYSK840439RECOMED CARDIAC OUTPUT METER 236067-K840523SERVOMED PULSE AMPLIFIER MODULE-206-K840524SERVOMED BASIC BEDSIDE UNIT SMV 110TPK840209SERVOMED MEDIVISION SCOPE SMV-235

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Related Devices (Code: DXJ)

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.

K212003ESSENZ Patient MonitorLivanova Deutschland, GmbHK212208Philips IntelliVue GuardianSoftware (Rev. E.0X)Philips Medizin Systeme Boeblingen GmbHK201162Essence 55SP Large Monitor SystemShenyang Torch-Bigtide Digital Technology Co., Ltd.K173107Vios Central Station Monitor Software, Vios Central Server SoftwareVios Medical, Inc.K180534Philips IntelliVue GuardianSoftwarePhilips Medizin Systeme Boeblingen GmbHK173381Nexxis ORBarco N.V.

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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