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FDA 510(k)

P460, DG32 ELECTROENCEPHALOGRAPH

K-Number: K896666 · 1990-02-16

ApplicantTeca, Inc.
Decision Date1990-02-16
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

P460, DG32 ELECTROENCEPHALOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Teca, Inc.. It received FDA 510(k) clearance on 1990-02-16 under 510(k) number K896666. 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 P460, DG32 ELECTROENCEPHALOGRAPH?

P460, DG32 ELECTROENCEPHALOGRAPH is a medical device that received FDA 510(k) clearance on 1990-02-16. The listed applicant is Teca, Inc.. The 510(k) number is K896666.

When did P460, DG32 ELECTROENCEPHALOGRAPH receive FDA 510(k) clearance?

P460, DG32 ELECTROENCEPHALOGRAPH received FDA 510(k) clearance on 1990-02-16, under 510(k) number K896666.

Who is the listed applicant for P460, DG32 ELECTROENCEPHALOGRAPH?

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

What is the FDA product code for P460, DG32 ELECTROENCEPHALOGRAPH?

The FDA product code for P460, DG32 ELECTROENCEPHALOGRAPH is GWQ.

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Other records listing Teca, Inc. 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.

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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