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FDA 510(k)

ELECTROENCEPHALOGRAPH ACCUTRACE 100

K-Number: K781041 · 1978-06-28

ApplicantBeckman Instruments, Inc.
Decision Date1978-06-28
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ELECTROENCEPHALOGRAPH ACCUTRACE 100 is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Instruments, Inc.. It received FDA 510(k) clearance on 1978-06-28 under 510(k) number K781041. The device is classified under product code GWQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROENCEPHALOGRAPH ACCUTRACE 100?

ELECTROENCEPHALOGRAPH ACCUTRACE 100 is a medical device that received FDA 510(k) clearance on 1978-06-28. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K781041.

When did ELECTROENCEPHALOGRAPH ACCUTRACE 100 receive FDA 510(k) clearance?

ELECTROENCEPHALOGRAPH ACCUTRACE 100 received FDA 510(k) clearance on 1978-06-28, under 510(k) number K781041.

Who is the listed applicant for ELECTROENCEPHALOGRAPH ACCUTRACE 100?

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

What is the FDA product code for ELECTROENCEPHALOGRAPH ACCUTRACE 100?

The FDA product code for ELECTROENCEPHALOGRAPH ACCUTRACE 100 is GWQ.

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Other records listing Beckman Instruments, Inc. as applicant

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Related Devices (Code: GWQ)

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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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