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FDA 510(k)

CEEGRAPH

K-Number: K895125 · 1989-12-22

ApplicantBio-Logic Systems Corp.
Decision Date1989-12-22
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CEEGRAPH 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 1989-12-22 under 510(k) number K895125. 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 CEEGRAPH?

CEEGRAPH is a medical device that received FDA 510(k) clearance on 1989-12-22. The listed applicant is Bio-Logic Systems Corp.. The 510(k) number is K895125.

When did CEEGRAPH receive FDA 510(k) clearance?

CEEGRAPH received FDA 510(k) clearance on 1989-12-22, under 510(k) number K895125.

Who is the listed applicant for CEEGRAPH?

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 CEEGRAPH?

The FDA product code for CEEGRAPH is GWQ.

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Other records listing Bio-Logic Systems Corp. 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.

K122496AUDX PRO OTOACOUSTIC EMISSIONS MEASUREMENT SYSTEMK121512SCOUT SPORT OTOACOUSTIC EMISSIONS MEASUREMENT SYSTEMK073626BIO-LOGIC MASTER II EVOKED RESPONSE SYSTEMK061744COCHLEA-SCAN / COCHLEA-SCAN PLUSK052066CEEGRAPH/SLEEPSCAN NETLINK TRAVELERK031352BIO-LOGIC INSERT EARPHONES

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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.

K261604Enobio Dx (Enobio Dx 8);Enobio Dx (Enobio Dx 20);Enobio Dx (Enobio Dx 32)Neuroelectrics Barcelona S.L.U.K260455New Wave SystemZeto, Inc.K233403Flexset SystemZeto, Inc.K231366Neuronaute PlusBioserenity SasK221959Q21Neurofield, Inc.K231457SPARK ScanSpark Neuro, Inc.

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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