Philips Biosensor BX100
FDA 510(k) K192875 · Philips Medical Systems
510(k) numberK192875
Submission
- Device name
- Philips Biosensor BX100
- Applicant
- Philips Medical Systems
Cambridge, MA, US - Received
- October 8, 2019
- Decision date
- April 16, 2020
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DRG – Transmitters And Receivers, Physiological Signal, Radiofrequency
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.2910
- Specialty
- Cardiovascular
Other 510(k)s with product code DRG
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261569 | UbiqVue 2AYe Cardiac System (UX2253)DRG · Traditional | Lifesignals, Inc. | 07/09/2026SE |
| K252984 | Perin Health System (PHD80060-2)DRG · Traditional | Perin Health Devices, LLC | 01/22/2026SE |
| K252440 | EasyTeleMed (2.0.2)DRG · Traditional | Ingeniars S.R.L. | 10/02/2025SE |
| K250259 | TeleRehab Aermos Cardiopulmonary RehabilitationDRG · Traditional | The ScottCare Corporation | 06/04/2025SE |
| K243837 | iBSMDRG · Traditional | Iorbit Digital Technologies Private Limited | 05/16/2025SE |
| K242018 | UbiqVue 2A Multi-parameter System (UX2550)DRG · Traditional | Lifesignals, Inc. | 11/12/2024SE |
| K241101 | BioButton SystemDRG · Traditional | Biointellisense, Inc. | 09/26/2024SE |
| K240251 | ANNE ChestDRG · Traditional | Sibel Health, Inc. | 06/03/2024SE |
| K223711 | ANNE OneDRG · Traditional | Sibel Health, Inc. | 08/10/2023SE |
| K220526 | HD+12, HD+15DRG · Traditional | Cardioline S.P.A | 05/15/2023SE |
More from Cardioline S.P.A
| 510(k) | Device | Decision |
|---|---|---|
| K212704 | Philips EPIQ Diagnostic Ultrasound System, Philips Affiniti Diagnostic Ultrasound SystemIYN · Traditional | 09/24/2021SE |
| K211597 | EPIQ Series Diagnostic Ultrasound System, Affiniti Series Diagnostic Ultrasound SystemIYN · Traditional | 09/08/2021SE |
| K210560 | Page Writer TC20 Cardiograph, Page Writer TC30 Cardiograph, Page Writer TC50…DPS · Special | 06/30/2021SE |
| K191738 | PageWriter TC20 Cardiograph, PageWriter TC30 Cardiograph, PageWriter TC50 Cardiograph…DPS · Traditional | 09/29/2020SE |
| K183387 | M3290B Patient Information Center iXMHX · Traditional | 08/06/2019SE |
| K180017 | MX40 Release C.01MHX · Special | 07/24/2018SE |
| K172226 | MX40 Release B.07MHX · Traditional | 11/09/2017SE |
| K163584 | M3290B Philips IntelliVue Information Center iXMHX · Traditional | 07/07/2017SE |
| K163649 | SureSigns VS3; SureSigns VS4DSJ · Special | 03/31/2017SE |
| K161164 | CareEvent inclusive of the CareEvent Mobile Application accessoryMSX · Traditional | 06/24/2016SE |
Questions and answers
When was Philips Biosensor BX100 cleared by the FDA?
Philips Biosensor BX100 (K192875) received a 510(k) decision of Substantially Equivalent on April 16, 2020, 191 days after the submission was received.
What is the product code of K192875?
The FDA product code is DRG – Transmitters And Receivers, Physiological Signal, Radiofrequency, a Class II (moderate risk) device regulated under 21 CFR 870.2910.