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FDA 510(k)

BIO-LOGIC CEEGRAPH 128-CHANNEL RECORDING SYSTEM

K-Number: K973883 · 1998-03-05

ApplicantBio-Logic Systems Corp.
Decision Date1998-03-05
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

BIO-LOGIC CEEGRAPH 128-CHANNEL RECORDING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Logic Systems Corp.. It received FDA 510(k) clearance on 1998-03-05 under 510(k) number K973883. 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 BIO-LOGIC CEEGRAPH 128-CHANNEL RECORDING SYSTEM?

BIO-LOGIC CEEGRAPH 128-CHANNEL RECORDING SYSTEM is a medical device that received FDA 510(k) clearance on 1998-03-05. The listed applicant is Bio-Logic Systems Corp.. The 510(k) number is K973883.

When did BIO-LOGIC CEEGRAPH 128-CHANNEL RECORDING SYSTEM receive FDA 510(k) clearance?

BIO-LOGIC CEEGRAPH 128-CHANNEL RECORDING SYSTEM received FDA 510(k) clearance on 1998-03-05, under 510(k) number K973883.

Who is the listed applicant for BIO-LOGIC CEEGRAPH 128-CHANNEL RECORDING SYSTEM?

The FDA 510(k) record lists Bio-Logic Systems Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIO-LOGIC CEEGRAPH 128-CHANNEL RECORDING SYSTEM?

The FDA product code for BIO-LOGIC CEEGRAPH 128-CHANNEL RECORDING SYSTEM is GWQ.

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Other records listing Bio-Logic Systems Corp. as applicant

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Related Devices (Code: GWQ)

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.

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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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