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FDA 510(k)

LME PATIENT MONITOR SMS 151

K-Number: K832013 · 1983-10-31

ApplicantLitton Medical Electronics
Decision Date1983-10-31
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LME PATIENT MONITOR SMS 151 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 1983-10-31 under 510(k) number K832013. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LME PATIENT MONITOR SMS 151?

LME PATIENT MONITOR SMS 151 is a medical device that received FDA 510(k) clearance on 1983-10-31. The listed applicant is Litton Medical Electronics. The 510(k) number is K832013.

When did LME PATIENT MONITOR SMS 151 receive FDA 510(k) clearance?

LME PATIENT MONITOR SMS 151 received FDA 510(k) clearance on 1983-10-31, under 510(k) number K832013.

Who is the listed applicant for LME PATIENT MONITOR SMS 151?

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 LME PATIENT MONITOR SMS 151?

The FDA product code for LME PATIENT MONITOR SMS 151 is DPS.

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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: DPS)

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.

K254255S-Patch CardioAIWellysis Corp.K252463SE-1202 Series Electrocardiograph (Model: SE-1202, SE-1202E)Edan Instruments, Inc.K251670MAC 7 Resting ECG Analysis SystemGe Medical Systems Information Technologies, Inc.K252361AccurECG Analysis System (v2.0)Accurkardia, Inc.K252474Withings BeamO (SCT02)WithingsK250569Cardiologs Holter PlatformPhilips France Commercial

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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