Edentec Digital Charter Model 3710
FDA 510(k) K910871 · Edentec Corp.
510(k) numberK910871
Submission
- Device name
- Edentec Digital Charter Model 3710
- Applicant
- Edentec Corp.
Eden Prairie, MN, US - Received
- March 1, 1991
- Decision date
- August 29, 1991
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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) | Device | Applicant | Decision |
|---|---|---|---|
| K912929 | Dash IVDSF · Traditional | Astro-Med, Inc. | 08/13/1991SE |
| K905856 | Model 556 MonitorDSF · Traditional | Ge Medical Systems Information Technologies | 01/11/1991SE |
| K902586 | Gri Lasergraph(Tm) ECG PaperDSF · Traditional | Gri Medical Products, Inc. | 06/22/1990SE |
| K902230 | Colorado Color Imaging RecorderDSF · Traditional | Honeywell, Inc. | 06/19/1990SE |
| K901385 | Gabriel Medical CLS Thermal RecorderDSF · Traditional | Gabriel Medical, Inc. | 05/09/1990SE |
| K895111 | Type 9541 Recorder, Paper ChartDSF · Traditional | S & W Medico Teknik | 01/26/1990SE |
| K894922 | WR3500 and WR3600 Series RecordersDSF · Traditional | Western Graphtec | 01/26/1990SE |
| K894736 | MT96000 Paper Chart RecorderDSF · Traditional | Astro-Med, Inc. | 12/13/1989SE |
| K894607 | PAQ10 Paper Chart RecorderDSF · Traditional | Protocol Systems, Inc. | 10/26/1989SE |
| K893561 | Edentrace 670 System Multichannel Recorder W/Oxim.DSF · Traditional | Edentec Corp. | 08/25/1989SE |
More from Edentec Corp.
| 510(k) | Device | Decision |
|---|---|---|
| K953363 | Oxiflow Digital RecorderBZQ · Traditional | 02/06/1996ST |
| K953540 | EeeBYD · Traditional | 08/25/1995SE |
| K921819 | Edentec Model 3710 I Digital PrinterBZQ · Traditional | 10/22/1993SE |
| K913749 | Edentrace Airflow 3171/SLEEP Lab Airflow 3170BZQ · Traditional | 07/02/1992SE |
| K910870 | Edentec Model 3711 Digital RecorderDRT · Traditional | 08/29/1991SE |
| K905575 | Modified Models 2000W and 2000W Option H Apnea MonBZQ · Traditional | 06/20/1991SE |
| K901060 | Edentec Model 2000W System 700 MonitorDQA · Traditional | 05/15/1990SE |
| K893561 | Edentrace 670 System Multichannel Recorder W/Oxim.DSF · Traditional | 08/25/1989SE |
| K892227 | Edentec Model 2001 Modular Memory Unit (Mmu)DSH · Traditional | 06/20/1989SE |
| K891540 | Edentec Model 2860 Pressure MeterBYE · Traditional | 06/01/1989SE |
Questions and answers
When was Edentec Digital Charter Model 3710 cleared by the FDA?
Edentec Digital Charter Model 3710 (K910871) received a 510(k) decision of Substantially Equivalent on August 29, 1991, 181 days after the submission was received.
What is the product code of K910871?
The FDA product code is DSF – Recorder, Paper Chart, a Class I (low risk) device regulated under 21 CFR 870.2810.