Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

EEG TELEPHONE TRANSMITTER, MODEL #T-7

K-Number: K813010 · 1981-11-16

ApplicantPharmaquest Corp.
Decision Date1981-11-16
Product CodeGYE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

EEG TELEPHONE TRANSMITTER, MODEL #T-7 is the device name listed in this FDA 510(k) record. The listed applicant is Pharmaquest Corp.. It received FDA 510(k) clearance on 1981-11-16 under 510(k) number K813010. 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 EEG TELEPHONE TRANSMITTER, MODEL #T-7?

EEG TELEPHONE TRANSMITTER, MODEL #T-7 is a medical device that received FDA 510(k) clearance on 1981-11-16. The listed applicant is Pharmaquest Corp.. The 510(k) number is K813010.

When did EEG TELEPHONE TRANSMITTER, MODEL #T-7 receive FDA 510(k) clearance?

EEG TELEPHONE TRANSMITTER, MODEL #T-7 received FDA 510(k) clearance on 1981-11-16, under 510(k) number K813010.

Who is the listed applicant for EEG TELEPHONE TRANSMITTER, MODEL #T-7?

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

What is the FDA product code for EEG TELEPHONE TRANSMITTER, MODEL #T-7?

The FDA product code for EEG TELEPHONE TRANSMITTER, MODEL #T-7 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Pharmaquest 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.

K945519FACE (FLUOROPHORE-ASSISTED-CARBOHYDRATE-ELECTROPHORESIS) URINARY CARBOHYDRATE ANALYSIS SYSTEMK833236TELEPHONE TRANSMITTER T-10 EEGK833880TELEPHONIC RECEIVER R-10 EEGK830705MINI LANCET-BLOOD LANCETK822976HYPOCOUNT AK822486HOME BLOOD GLUCOSE MONITOR

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.

K963195WIRELESS EEG RECORDING SYSTEM MODEL W32Cme Telemetrix, Inc.K970659DT-24 TELEPHONIC EEG TRANSMITTER/DR-24 TELEPHONIC EEG RECEIVERTelediagnostic Systems, Inc.K895895MODEL 219 TELEMETRY SYSTEMMennen Medical, Inc.K891405BMS-2000 MOBILE EEG SYSTEMBuckman Co., Inc.K885328RS-10 TELEPHONIC POLYSOMNOGRAPHY RECEIVERTelediagnostic Systems, Inc.K883947ISO-100 ISOLATION AMPLIFIERTelediagnostic Systems, 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.

↑