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FDA 510(k)

BRENTWOOD EZ SCAN 200 AMBULATORY ECG

K-Number: K842976 · 1985-03-01

ApplicantBrentwood Instruments, Inc.
Decision Date1985-03-01
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BRENTWOOD EZ SCAN 200 AMBULATORY ECG is the device name listed in this FDA 510(k) record. The listed applicant is Brentwood Instruments, Inc.. It received FDA 510(k) clearance on 1985-03-01 under 510(k) number K842976. 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 BRENTWOOD EZ SCAN 200 AMBULATORY ECG?

BRENTWOOD EZ SCAN 200 AMBULATORY ECG is a medical device that received FDA 510(k) clearance on 1985-03-01. The listed applicant is Brentwood Instruments, Inc.. The 510(k) number is K842976.

When did BRENTWOOD EZ SCAN 200 AMBULATORY ECG receive FDA 510(k) clearance?

BRENTWOOD EZ SCAN 200 AMBULATORY ECG received FDA 510(k) clearance on 1985-03-01, under 510(k) number K842976.

Who is the listed applicant for BRENTWOOD EZ SCAN 200 AMBULATORY ECG?

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

What is the FDA product code for BRENTWOOD EZ SCAN 200 AMBULATORY ECG?

The FDA product code for BRENTWOOD EZ SCAN 200 AMBULATORY ECG is DSI.

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Other records listing Brentwood Instruments, Inc. as applicant

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Related Devices (Code: DSI)

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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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