Centurion Chart Recorder

FDA 510(k) K822432 · Clinical Data, Inc.

Substantially Equivalent

510(k) numberK822432

Submission

Device name
Centurion Chart Recorder
Applicant
Clinical Data, Inc.
Walker, MI, US
Received
August 12, 1982
Decision date
November 1, 1982
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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K905856Model 556 MonitorDSF · Traditional Ge Medical Systems Information Technologies01/11/1991SE
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

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Questions and answers

When was Centurion Chart Recorder cleared by the FDA?

Centurion Chart Recorder (K822432) received a 510(k) decision of Substantially Equivalent on November 1, 1982, 81 days after the submission was received.

What is the product code of K822432?

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