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FDA 510(k)

FCP-11ECG

K-Number: K842169 · 1984-03-13

ApplicantBrentwood Instruments, Inc.
Decision Date1984-03-13
Product Code
DecisionUnknown

Device Summary

FCP-11ECG 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 1984-03-13 under 510(k) number K842169. FDA Decision: Unknown.

Frequently Asked Questions

What is the FCP-11ECG?

FCP-11ECG is a medical device that received FDA 510(k) clearance on 1984-03-13. The listed applicant is Brentwood Instruments, Inc.. The 510(k) number is K842169.

When did FCP-11ECG receive FDA 510(k) clearance?

FCP-11ECG received FDA 510(k) clearance on 1984-03-13, under 510(k) number K842169.

Who is the listed applicant for FCP-11ECG?

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

Other records listing Brentwood 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.

K896924SPIROSCAN 4000K882366RHYTHMSCAN HR HOLTER RECORDERK871572RHYTHMSCANK860024FUKUDA DENSHI CARDIMAX FCP-211K853979CARDIMAX FX-1164K854505CARDIMAX FX-406U

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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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