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FDA 510(k)

BIO-LOGIC CEEGRAPH NETLINK

K-Number: K002570 · 2000-09-14

ApplicantBio-Logic Systems Corp.
Decision Date2000-09-14
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

BIO-LOGIC CEEGRAPH NETLINK 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 2000-09-14 under 510(k) number K002570. 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 NETLINK?

BIO-LOGIC CEEGRAPH NETLINK is a medical device that received FDA 510(k) clearance on 2000-09-14. The listed applicant is Bio-Logic Systems Corp.. The 510(k) number is K002570.

When did BIO-LOGIC CEEGRAPH NETLINK receive FDA 510(k) clearance?

BIO-LOGIC CEEGRAPH NETLINK received FDA 510(k) clearance on 2000-09-14, under 510(k) number K002570.

Who is the listed applicant for BIO-LOGIC CEEGRAPH NETLINK?

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 NETLINK?

The FDA product code for BIO-LOGIC CEEGRAPH NETLINK is GWQ.

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Other records listing Bio-Logic Systems Corp. as applicant

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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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