FDA 510(k)

EKG, ECG KENZ, ECG 302

K-Number: K896771 · 1990-02-26

ApplicantCambridge Medical Instruments, Inc.

Decision Date1990-02-26

Product CodeDSI

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

EKG, ECG KENZ, ECG 302 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 1990-02-26 under 510(k) number K896771. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EKG, ECG KENZ, ECG 302?

EKG, ECG KENZ, ECG 302 is a medical device that received FDA 510(k) clearance on 1990-02-26. The listed applicant is Cambridge Medical Instruments, Inc.. The 510(k) number is K896771.

When did EKG, ECG KENZ, ECG 302 receive FDA 510(k) clearance?

EKG, ECG KENZ, ECG 302 received FDA 510(k) clearance on 1990-02-26, under 510(k) number K896771.

Who is the listed applicant for EKG, ECG KENZ, ECG 302?

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 EKG, ECG KENZ, ECG 302?

The FDA product code for EKG, ECG KENZ, ECG 302 is DSI.

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 303 K895961MODEL MC6500 ELECTROCARDIOGRAPH K883454MC6700 MULTI-CHANNEL ELECTROCARDIOGRAPH K871993MC 6000 MULTI-CHANNEL ELECTROCARDIOGRAPH K862748MODEL SC-1000 ELECTROCARDIOGRAPH SPECIFICATION K854282PREVIEW XT

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Official Source

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