Dash IV
FDA 510(k) K912929 · Astro-Med, Inc.
510(k) numberK912929
Submission
- Device name
- Dash IV
- Applicant
- Astro-Med, Inc.
West Warwick, RI, US - Received
- July 5, 1991
- Decision date
- August 13, 1991
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
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 |
| 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 |
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| K934644 | K3 SystemDRT · Traditional | 11/01/1994SE |
| K896164 | ASC-954 Integrator AmplifierGWK · Traditional | 01/22/1990SE |
| K894295 | Astro-Med ASC-951 Pressure ProcessorDRQ · Traditional | 01/18/1990SE |
| K894736 | MT96000 Paper Chart RecorderDSF · Traditional | 12/13/1989SE |
| K894735 | ASC-952 Physiological AmplifierDRR · Traditional | 09/18/1989SE |
Questions and answers
When was Dash IV cleared by the FDA?
Dash IV (K912929) received a 510(k) decision of Substantially Equivalent on August 13, 1991, 39 days after the submission was received.
What is the product code of K912929?
The FDA product code is DSF – Recorder, Paper Chart, a Class I (low risk) device regulated under 21 CFR 870.2810.