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FDA 510(k)

CENTRAL STATION MONITORING SYSTEMS

K-Number: K811121 · 1981-06-30

ApplicantCambridge Instruments, Inc.
Decision Date1981-06-30
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CENTRAL STATION MONITORING SYSTEMS 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 1981-06-30 under 510(k) number K811121. 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 CENTRAL STATION MONITORING SYSTEMS?

CENTRAL STATION MONITORING SYSTEMS is a medical device that received FDA 510(k) clearance on 1981-06-30. The listed applicant is Cambridge Instruments, Inc.. The 510(k) number is K811121.

When did CENTRAL STATION MONITORING SYSTEMS receive FDA 510(k) clearance?

CENTRAL STATION MONITORING SYSTEMS received FDA 510(k) clearance on 1981-06-30, under 510(k) number K811121.

Who is the listed applicant for CENTRAL STATION MONITORING SYSTEMS?

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 CENTRAL STATION MONITORING SYSTEMS?

The FDA product code for CENTRAL STATION MONITORING SYSTEMS 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.

K811062CAMPBRIDGE COMPUTRACEK8032294-CHANNEL ECG TELEMETRY MON. SYST. #3045K801224CAMBRIDGE CARDIAC DIAGNOSTIC SYSTEMK800566CAMBRIDGE VS-550 ELECTROCARDIOGRAPHK792661TREADMILL 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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