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FDA 510(k)

ELECTROCARDIOGRAPH (MODEL VS-4B)

K-Number: K760926 · 1976-11-09

ApplicantCambridge Instruments, Inc.
Decision Date1976-11-09
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTROCARDIOGRAPH (MODEL VS-4B) is the device name listed in this FDA 510(k) record. The listed applicant is Cambridge Instruments, Inc.. It received FDA 510(k) clearance on 1976-11-09 under 510(k) number K760926. 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 ELECTROCARDIOGRAPH (MODEL VS-4B)?

ELECTROCARDIOGRAPH (MODEL VS-4B) is a medical device that received FDA 510(k) clearance on 1976-11-09. The listed applicant is Cambridge Instruments, Inc.. The 510(k) number is K760926.

When did ELECTROCARDIOGRAPH (MODEL VS-4B) receive FDA 510(k) clearance?

ELECTROCARDIOGRAPH (MODEL VS-4B) received FDA 510(k) clearance on 1976-11-09, under 510(k) number K760926.

Who is the listed applicant for ELECTROCARDIOGRAPH (MODEL VS-4B)?

The FDA 510(k) record lists Cambridge Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTROCARDIOGRAPH (MODEL VS-4B)?

The FDA product code for ELECTROCARDIOGRAPH (MODEL VS-4B) is DPS.

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Other records listing Cambridge Instruments, Inc. 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.

K811121CENTRAL STATION MONITORING SYSTEMSK811062CAMPBRIDGE COMPUTRACEK8032294-CHANNEL ECG TELEMETRY MON. SYST. #3045K801224CAMBRIDGE CARDIAC DIAGNOSTIC SYSTEMK800566CAMBRIDGE VS-550 ELECTROCARDIOGRAPHK792661TREADMILL MODEL 3060

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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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