Cardiocap(Tm) DR-104 Reporter
FDA 510(k) K885058 · Datex Division Instrumentarium Corp.
510(k) numberK885058
Submission
- Device name
- Cardiocap(Tm) DR-104 Reporter
- Applicant
- Datex Division Instrumentarium Corp.
Helsinki, Finland, FI - Received
- December 7, 1988
- Decision date
- July 14, 1989
- 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 |
|---|---|---|
| K953175 | AS/3 Estpr ModuleMLD · Traditional | 02/06/1997SE |
| K961247 | AS/3 Light MonitorDPS · Traditional | 10/23/1996SE |
| K943458 | AS/3 Airway ModuleCBS · Traditional | 02/14/1995SE |
| K945234 | AS/3 Memory Module, M0MEMBSZ · Traditional | 01/27/1995SE |
| K933156 | Datex AS/3 Patient MonitorDPS · Traditional | 12/30/1994SE |
| K933285 | Datex AS/3 TM Anaesthesia MonitorBSZ · Traditional | 11/14/1994SE |
| K943456 | AS/3 Nellcor Compatible Saturation Moodule, M-NsatDQA · Traditional | 10/17/1994SE |
| K923172 | Anaesthesia Record KeeperBSZ · Traditional | 08/09/1994SE |
| K935477 | AS/3(TM) Anesthesia Monitor Syst Interface BoardCCK · Traditional | 08/01/1994SE |
| K943457 | AS/3 Pressure Temperature Module, M-PtDSK · Traditional | 07/27/1994SE |
Questions and answers
When was Cardiocap(Tm) DR-104 Reporter cleared by the FDA?
Cardiocap(Tm) DR-104 Reporter (K885058) received a 510(k) decision of Substantially Equivalent on July 14, 1989, 219 days after the submission was received.
What is the product code of K885058?
The FDA product code is DSF – Recorder, Paper Chart, a Class I (low risk) device regulated under 21 CFR 870.2810.