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FDA 510(k)

SERVOMED BASIC BEDSIDE UNIT SMV 110TP

K-Number: K840524 · 1984-10-26

ApplicantLitton Medical Electronics
Decision Date1984-10-26
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SERVOMED BASIC BEDSIDE UNIT SMV 110TP 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 1984-10-26 under 510(k) number K840524. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERVOMED BASIC BEDSIDE UNIT SMV 110TP?

SERVOMED BASIC BEDSIDE UNIT SMV 110TP is a medical device that received FDA 510(k) clearance on 1984-10-26. The listed applicant is Litton Medical Electronics. The 510(k) number is K840524.

When did SERVOMED BASIC BEDSIDE UNIT SMV 110TP receive FDA 510(k) clearance?

SERVOMED BASIC BEDSIDE UNIT SMV 110TP received FDA 510(k) clearance on 1984-10-26, under 510(k) number K840524.

Who is the listed applicant for SERVOMED BASIC BEDSIDE UNIT SMV 110TP?

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 110TP?

The FDA product code for SERVOMED BASIC BEDSIDE UNIT SMV 110TP is DRT.

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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-K840209SERVOMED MEDIVISION SCOPE SMV-235K840832SERVOMED OXCARDIORE SPIROGRAPH 324/111

View all 38 devices →

Related Devices (Code: DRT)

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.

K254058DistaSense(TM) (v1)Life Detection TechnologiesK261286The Circadia C300 System (C300)Circadia Health, Inc.K252676The Circadia C300 System (C300)Circadia Health, Inc.K253388Sleepiz One+ (Model 2.5)Sleepiz AGK251364Sleepiz One+ (2.5)Sleepiz AGK234003The Circadia C200 SystemCircadia Technologies, Ltd.

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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