Edentec Model 4700 Scanner

FDA 510(k) K884388 · Edentec Corp.

Substantially Equivalent

510(k) numberK884388

Submission

Device name
Edentec Model 4700 Scanner
Applicant
Edentec Corp.
Eden Prairie, MN, US
Received
October 18, 1988
Decision date
January 10, 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

Other 510(k)s with product code DSF

510(k)DeviceApplicantDecision
K910871Edentec Digital Charter Model 3710DSF · Traditional Edentec Corp.08/29/1991SE
K912929Dash IVDSF · Traditional Astro-Med, Inc.08/13/1991SE
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

More from Protocol Systems, Inc.

510(k)DeviceDecision
K953363Oxiflow Digital RecorderBZQ · Traditional 02/06/1996ST
K953540EeeBYD · Traditional 08/25/1995SE
K921819Edentec Model 3710 I Digital PrinterBZQ · Traditional 10/22/1993SE
K913749Edentrace Airflow 3171/SLEEP Lab Airflow 3170BZQ · Traditional 07/02/1992SE
K910871Edentec Digital Charter Model 3710DSF · Traditional 08/29/1991SE
K910870Edentec Model 3711 Digital RecorderDRT · Traditional 08/29/1991SE
K905575Modified Models 2000W and 2000W Option H Apnea MonBZQ · Traditional 06/20/1991SE
K901060Edentec Model 2000W System 700 MonitorDQA · Traditional 05/15/1990SE
K893561Edentrace 670 System Multichannel Recorder W/Oxim.DSF · Traditional 08/25/1989SE
K892227Edentec Model 2001 Modular Memory Unit (Mmu)DSH · Traditional 06/20/1989SE

Questions and answers

When was Edentec Model 4700 Scanner cleared by the FDA?

Edentec Model 4700 Scanner (K884388) received a 510(k) decision of Substantially Equivalent on January 10, 1989, 84 days after the submission was received.

What is the product code of K884388?

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