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FDA 510(k)

MC6700 MULTI-CHANNEL ELECTROCARDIOGRAPH

K-Number: K883454 · 1989-01-25

ApplicantCambridge Medical Instruments, Inc.
Decision Date1989-01-25
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MC6700 MULTI-CHANNEL ELECTROCARDIOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Cambridge Medical Instruments, Inc.. It received FDA 510(k) clearance on 1989-01-25 under 510(k) number K883454. 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 MC6700 MULTI-CHANNEL ELECTROCARDIOGRAPH?

MC6700 MULTI-CHANNEL ELECTROCARDIOGRAPH is a medical device that received FDA 510(k) clearance on 1989-01-25. The listed applicant is Cambridge Medical Instruments, Inc.. The 510(k) number is K883454.

When did MC6700 MULTI-CHANNEL ELECTROCARDIOGRAPH receive FDA 510(k) clearance?

MC6700 MULTI-CHANNEL ELECTROCARDIOGRAPH received FDA 510(k) clearance on 1989-01-25, under 510(k) number K883454.

Who is the listed applicant for MC6700 MULTI-CHANNEL ELECTROCARDIOGRAPH?

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

What is the FDA product code for MC6700 MULTI-CHANNEL ELECTROCARDIOGRAPH?

The FDA product code for MC6700 MULTI-CHANNEL ELECTROCARDIOGRAPH is DPS.

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Other records listing Cambridge Medical 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.

K896772EKG, ECG KENZ, ECG 303K896771EKG, ECG KENZ, ECG 302K895961MODEL MC6500 ELECTROCARDIOGRAPHK871993MC 6000 MULTI-CHANNEL ELECTROCARDIOGRAPHK862748MODEL SC-1000 ELECTROCARDIOGRAPH SPECIFICATIONK854282PREVIEW XT

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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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