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FDA 510(k)

MULTISCRIPTOR EK VARIOUS #43

K-Number: K832015 · 1983-10-31

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

Device Summary

MULTISCRIPTOR EK VARIOUS #43 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 K832015. 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 MULTISCRIPTOR EK VARIOUS #43?

MULTISCRIPTOR EK VARIOUS #43 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 K832015.

When did MULTISCRIPTOR EK VARIOUS #43 receive FDA 510(k) clearance?

MULTISCRIPTOR EK VARIOUS #43 received FDA 510(k) clearance on 1983-10-31, under 510(k) number K832015.

Who is the listed applicant for MULTISCRIPTOR EK VARIOUS #43?

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 MULTISCRIPTOR EK VARIOUS #43?

The FDA product code for MULTISCRIPTOR EK VARIOUS #43 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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