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FDA 510(k)

BRACKMANN EMG MONITORING SYSTEM

K-Number: K895838 · 1990-03-27

ApplicantWr Medical Electronics Co.
Decision Date1990-03-27
Product CodeETN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

BRACKMANN EMG MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Wr Medical Electronics Co.. It received FDA 510(k) clearance on 1990-03-27 under 510(k) number K895838. The device is classified under product code ETN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRACKMANN EMG MONITORING SYSTEM?

BRACKMANN EMG MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 1990-03-27. The listed applicant is Wr Medical Electronics Co.. The 510(k) number is K895838.

When did BRACKMANN EMG MONITORING SYSTEM receive FDA 510(k) clearance?

BRACKMANN EMG MONITORING SYSTEM received FDA 510(k) clearance on 1990-03-27, under 510(k) number K895838.

Who is the listed applicant for BRACKMANN EMG MONITORING SYSTEM?

The FDA 510(k) record lists Wr Medical Electronics Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BRACKMANN EMG MONITORING SYSTEM?

The FDA product code for BRACKMANN EMG MONITORING SYSTEM is ETN.

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Other records listing Wr Medical Electronics Co. as applicant

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Related Devices (Code: ETN)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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