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FDA 510(k)

MODEL T-6 EEG TELEPHONE TRANSMITTER

K-Number: K802656 · 1980-11-26

Decision Date1980-11-26
Product CodeGYE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MODEL T-6 EEG TELEPHONE TRANSMITTER is the device name listed in this FDA 510(k) record. The listed applicant is Telediagnostic Systems, Inc.. It received FDA 510(k) clearance on 1980-11-26 under 510(k) number K802656. The device is classified under product code GYE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL T-6 EEG TELEPHONE TRANSMITTER?

MODEL T-6 EEG TELEPHONE TRANSMITTER is a medical device that received FDA 510(k) clearance on 1980-11-26. The listed applicant is Telediagnostic Systems, Inc.. The 510(k) number is K802656.

When did MODEL T-6 EEG TELEPHONE TRANSMITTER receive FDA 510(k) clearance?

MODEL T-6 EEG TELEPHONE TRANSMITTER received FDA 510(k) clearance on 1980-11-26, under 510(k) number K802656.

Who is the listed applicant for MODEL T-6 EEG TELEPHONE TRANSMITTER?

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

What is the FDA product code for MODEL T-6 EEG TELEPHONE TRANSMITTER?

The FDA product code for MODEL T-6 EEG TELEPHONE TRANSMITTER is GYE.

Related Clinical Trials

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.

Other records listing Telediagnostic Systems, Inc. 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.

View all 14 devices →

Related Devices (Code: GYE)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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