MT96000 Paper Chart Recorder

FDA 510(k) K894736 · Astro-Med, Inc.

Substantially Equivalent

510(k) numberK894736

Submission

Device name
MT96000 Paper Chart Recorder
Applicant
Astro-Med, Inc.
West Warwick, RI, US
Received
July 27, 1989
Decision date
December 13, 1989
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
K894607PAQ10 Paper Chart RecorderDSF · Traditional Protocol Systems, Inc.10/26/1989SE
K893561Edentrace 670 System Multichannel Recorder W/Oxim.DSF · Traditional Edentec Corp.08/25/1989SE

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Questions and answers

When was MT96000 Paper Chart Recorder cleared by the FDA?

MT96000 Paper Chart Recorder (K894736) received a 510(k) decision of Substantially Equivalent on December 13, 1989, 139 days after the submission was received.

What is the product code of K894736?

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