Printer, Digital
FDA 510(k) K781115 · Output, Inc.
510(k) numberK781115
Submission
- Device name
- Printer, Digital
- Applicant
- Output, Inc.
Mchenry, IL, US - Received
- July 3, 1978
- Decision date
- October 6, 1978
- 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 |
|---|---|---|---|
| K910871 | Edentec Digital Charter Model 3710DSF · Traditional | Edentec Corp. | 08/29/1991SE |
| 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 |
More from Protocol Systems, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K800360 | Output Digital Display Module, Mod. 611DSK · Traditional | 02/29/1980SE |
| K780356 | Output Digital Display Module, Model 401DSK · Traditional | 05/31/1978SE |
| K770987 | Nerve Stimulator, Molel No. FB-800GZI · Traditional | 06/14/1977SE |
| K760614 | Peripheral Nerve StimulatorBXN · Traditional | 11/19/1976SE |
Questions and answers
When was Printer, Digital cleared by the FDA?
Printer, Digital (K781115) received a 510(k) decision of Substantially Equivalent on October 6, 1978, 95 days after the submission was received.
What is the product code of K781115?
The FDA product code is DSF – Recorder, Paper Chart, a Class I (low risk) device regulated under 21 CFR 870.2810.