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FDA 510(k)

TELEPHONIC RECEIVER R-10 EEG

K-Number: K833880 · 1983-11-29

ApplicantPharmaquest Corp.
Decision Date1983-11-29
Product CodeGYE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TELEPHONIC RECEIVER R-10 EEG is the device name listed in this FDA 510(k) record. The listed applicant is Pharmaquest Corp.. It received FDA 510(k) clearance on 1983-11-29 under 510(k) number K833880. 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 TELEPHONIC RECEIVER R-10 EEG?

TELEPHONIC RECEIVER R-10 EEG is a medical device that received FDA 510(k) clearance on 1983-11-29. The listed applicant is Pharmaquest Corp.. The 510(k) number is K833880.

When did TELEPHONIC RECEIVER R-10 EEG receive FDA 510(k) clearance?

TELEPHONIC RECEIVER R-10 EEG received FDA 510(k) clearance on 1983-11-29, under 510(k) number K833880.

Who is the listed applicant for TELEPHONIC RECEIVER R-10 EEG?

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 TELEPHONIC RECEIVER R-10 EEG?

The FDA product code for TELEPHONIC RECEIVER R-10 EEG is GYE.

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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 EEGK830705MINI LANCET-BLOOD LANCETK822976HYPOCOUNT AK822486HOME BLOOD GLUCOSE MONITORK820248RODDER VOLUME VENTILATOR

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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.

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