MODEL AFR EEG TELEPHONE RECEIVER
K-Number: K802657 · 1980-11-12
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Device Summary
Frequently Asked Questions
What is the MODEL AFR EEG TELEPHONE RECEIVER?
MODEL AFR EEG TELEPHONE RECEIVER is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Telediagnostic Systems, Inc.. The 510(k) number is K802657.
When did MODEL AFR EEG TELEPHONE RECEIVER receive FDA 510(k) clearance?
MODEL AFR EEG TELEPHONE RECEIVER received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802657.
Who is the listed applicant for MODEL AFR EEG TELEPHONE RECEIVER?
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 AFR EEG TELEPHONE RECEIVER?
The FDA product code for MODEL AFR EEG TELEPHONE RECEIVER 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.
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
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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