Recording Accessory for G-2000 EKG Mach. GMP-40 Re

FDA 510(k) K850365 · Eaton Medical Group

Substantially Equivalent

510(k) numberK850365

Submission

Device name
Recording Accessory for G-2000 EKG Mach. GMP-40 Re
Applicant
Eaton Medical Group
Eaton, MI, US
Received
January 30, 1985
Decision date
April 9, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DSF – Recorder, Paper Chart
Device class
Class I (low risk)
Regulation
21 CFR 870.2810
Specialty
Cardiovascular

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K902586Gri Lasergraph(Tm) ECG PaperDSF · Traditional Gri Medical Products, Inc.06/22/1990SE
K902230Colorado Color Imaging RecorderDSF · Traditional Honeywell, Inc.06/19/1990SE
K901385Gabriel Medical CLS Thermal RecorderDSF · Traditional Gabriel Medical, Inc.05/09/1990SE
K895111Type 9541 Recorder, Paper ChartDSF · Traditional S & W Medico Teknik01/26/1990SE
K894922WR3500 and WR3600 Series RecordersDSF · Traditional Western Graphtec01/26/1990SE
K894736MT96000 Paper Chart RecorderDSF · Traditional Astro-Med, Inc.12/13/1989SE
K894607PAQ10 Paper Chart RecorderDSF · Traditional Protocol Systems, Inc.10/26/1989SE

More from Protocol Systems, Inc.

510(k)DeviceDecision
K851623Model TRC-40 Telemetry Reciever ModuleDXH · Traditional 01/22/1986SE
K851624Model TT-185 Telemetry TransmitterDXH · Traditional 01/14/1986SE
K851625SCX-10 Single Channel Recorder Access. for G-2000DSF · Traditional 11/19/1985SE
K851632PCX-100 Patient Input LeadwireDRW · Traditional 11/08/1985SE
K851627KBX-20 Outboard Keyboard Access. for G-2000 ElectrDRW · Traditional 11/08/1985SE
K851631TMX-C1/C2 Tradmill Controller Access.IOL · Traditional 07/15/1985SE
K851630TMX-80 TreadmillIOL · Traditional 07/09/1985SE
K851629TMX-70 TreadmillIOL · Traditional 07/09/1985SE
K851628RMG-9 9 Remote Monitor Access. for G-2000 ElectroDXJ · Traditional 06/27/1985SE
K851633CC-100 Clock/Calander Module Access. for G-2000 ElDPS · Traditional 06/26/1985SE

Questions and answers

When was Recording Accessory for G-2000 EKG Mach. GMP-40 Re cleared by the FDA?

Recording Accessory for G-2000 EKG Mach. GMP-40 Re (K850365) received a 510(k) decision of Substantially Equivalent on April 9, 1985, 69 days after the submission was received.

What is the product code of K850365?

The FDA product code is DSF – Recorder, Paper Chart, a Class I (low risk) device regulated under 21 CFR 870.2810.