M10 EEG Monitor Scope

FDA 510(k) K871120 · Telediagnostic Systems, Inc.

Substantially Equivalent

510(k) numberK871120

Submission

Device name
M10 EEG Monitor Scope
Applicant
Telediagnostic Systems, Inc.
San Francisco, CA, US
Received
March 19, 1987
Decision date
May 1, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GYE – Encephalogram Telemetry System
Device class
Class II (moderate risk)
Regulation
21 CFR 882.1855
Specialty
Neurology

Other 510(k)s with product code GYE

510(k)DeviceApplicantDecision
K963195Wireless EEG Recording System Model W32GYE · Traditional Cme Telemetrix, Inc.07/29/1997SE
K970659DT-24 Telephonic EEG TRANSMITTER/DR-24 Telephonic EEG ReceiverGYE · Traditional Telediagnostic Systems, Inc.05/16/1997SE
K895895Model 219 Telemetry SystemGYE · Traditional Mennen Medical, Inc.02/22/1990SE
K891405BMS-2000 Mobile EEG SystemGYE · Traditional Buckman Co., Inc.08/02/1989SE
K885328RS-10 Telephonic Polysomnography ReceiverGYE · Traditional Telediagnostic Systems, Inc.03/22/1989SE
K883947ISO-100 Isolation AmplifierGYE · Traditional Telediagnostic Systems, Inc.12/05/1988SE
K883461Dad 16S, Data Acquistion Device 16 Ch. SeriesGYE · Traditional Biohm, Inc.11/30/1988SE
K874257S-10 Telephonic PolysomnographGYE · Traditional Telediagnostic Systems, Inc.12/11/1987SE
K860128Modac-Xxxx Intensive Monitoring of EEGGYE · Traditional Grass-Telefactor Product Group03/27/1986SE
K833880Telephonic Receiver R-10 EEGGYE · Traditional Pharmaquest Corp.11/29/1983SE

More from Pharmaquest Corp.

510(k)DeviceDecision
K071661Alphaone Biofeedback SystemHCC · Traditional 09/05/2007SE
K022249Nightron Polysomnography SystemOLV · Traditional 12/31/2002SE
K970659DT-24 Telephonic EEG TRANSMITTER/DR-24 Telephonic EEG ReceiverGYE · Traditional 05/16/1997SE
K904328Vista Polysomnography Computer SystemGWK · Traditional 06/18/1991SE
K904222Vista Graph Polysomnography AmplifierGWL · Traditional 01/18/1991SE
K885328RS-10 Telephonic Polysomnography ReceiverGYE · Traditional 03/22/1989SE
K884891OC-100 Oximeter Interface CalibratorDQA · Traditional 12/28/1988SE
K883947ISO-100 Isolation AmplifierGYE · Traditional 12/05/1988SE
K874257S-10 Telephonic PolysomnographGYE · Traditional 12/11/1987SE
K810872EEG Telephone Receiver Model #Afr-JDXH · Traditional 05/01/1981SE

Questions and answers

When was M10 EEG Monitor Scope cleared by the FDA?

M10 EEG Monitor Scope (K871120) received a 510(k) decision of Substantially Equivalent on May 1, 1987, 43 days after the submission was received.

What is the product code of K871120?

The FDA product code is GYE – Encephalogram Telemetry System, a Class II (moderate risk) device regulated under 21 CFR 882.1855.