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FDA 510(k)

CAMBRIDGE VS-550 ELECTROCARDIOGRAPH

K-Number: K800566 · 1980-04-08

ApplicantCambridge Instruments, Inc.
Decision Date1980-04-08
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CAMBRIDGE VS-550 ELECTROCARDIOGRAPH 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 1980-04-08 under 510(k) number K800566. 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 CAMBRIDGE VS-550 ELECTROCARDIOGRAPH?

CAMBRIDGE VS-550 ELECTROCARDIOGRAPH is a medical device that received FDA 510(k) clearance on 1980-04-08. The listed applicant is Cambridge Instruments, Inc.. The 510(k) number is K800566.

When did CAMBRIDGE VS-550 ELECTROCARDIOGRAPH receive FDA 510(k) clearance?

CAMBRIDGE VS-550 ELECTROCARDIOGRAPH received FDA 510(k) clearance on 1980-04-08, under 510(k) number K800566.

Who is the listed applicant for CAMBRIDGE VS-550 ELECTROCARDIOGRAPH?

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 CAMBRIDGE VS-550 ELECTROCARDIOGRAPH?

The FDA product code for CAMBRIDGE VS-550 ELECTROCARDIOGRAPH 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 SYSTEMK792661TREADMILL MODEL 3060K791201SCINTISTRESS SYSTEM

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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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