Stat-Scan
FDA 510(k) K822093 · Survival Technology, Inc.
510(k) numberK822093
Submission
- Device name
- Stat-Scan
- Applicant
- Survival Technology, Inc.
Mchenry, IL, US - Received
- July 16, 1982
- Decision date
- September 21, 1982
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- DXG – Computer, Diagnostic, Pre-Programmed, Single-Function
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1435
- Specialty
- Cardiovascular
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|---|---|---|---|
| K253092 | Argos Infinity (Rev. 1.0)DXG · Traditional | Retia Medical Systems, Inc. | 02/13/2026SE |
| K251275 | VitalStream ART Connect; VitalStream-HemoDXG · Traditional | Caretaker Medical | 09/26/2025SE |
| K232048 | Cogent Hemodynamic Monitoring System; Cogent HMSDXG · Traditional | Icu Medical | 12/20/2023SE |
| K212529 | Hypotension Decision Assist Model HDA-OR2DXG · Special | Directed Systems, Ltd. | 11/23/2021SE |
| K192169 | PulsioFlex Monitoring System with ProAQT SensorDXG · Traditional | Pulsion Medical Systems SE | 04/30/2020SE |
| K193179 | EV1000 Clinical PlatformDXG · Special | Edwards Lifesciences, LLC | 12/17/2019SE |
| K190955 | Hypotension Decision AssistDXG · Traditional | Directed Systems, Ltd. | 11/27/2019SE |
| K181372 | ArgosDXG · Traditional | Retia Medical, LLC | 12/13/2018SE |
| K172259 | PulsioFlex Monitoring SystemDXG · Traditional | Pulsion Medical Systems SE | 01/18/2018SE |
| K163334 | LiDCOunity v2 Hemodynamic MonitorDXG · Traditional | Lidco, Ltd. | 06/05/2017SE |
More from Lidco, Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K925535 | Cardiobeeper(R) Cb-IiaDXH · Traditional | 01/28/1993SE |
| K894799 | Cardiobeeper Memory Monitor CB 600 SeriesDXH · Traditional | 10/03/1989SE |
| K890461 | Cardiobeeper IVDXH · Traditional | 02/23/1989SE |
| K883843 | Cardiobeeper IIDXH · Traditional | 11/09/1988SE |
| K883614 | Cytoguard(R)FMF · Traditional | 09/15/1988SE |
| K880300 | Cardiobeeper(R) IIIDXH · Traditional | 05/12/1988SE |
| K844966 | Cardiobeeper Profile MonitorDXH · Traditional | 02/08/1985SE |
| K813101 | Cardiobeeper Memory MonitorDXY · Traditional | 11/27/1981SE |
| K772178 | Pacer Monitor, Pulse WidthDXH · Traditional | 12/08/1977SE |
Questions and answers
When was Stat-Scan cleared by the FDA?
Stat-Scan (K822093) received a 510(k) decision of Substantially Equivalent on September 21, 1982, 67 days after the submission was received.
What is the product code of K822093?
The FDA product code is DXG – Computer, Diagnostic, Pre-Programmed, Single-Function, a Class II (moderate risk) device regulated under 21 CFR 870.1435.