BP-200 Plus
FDA 510(k) K063814 · Schiller AG
510(k) numberK063814
Submission
- Device name
- BP-200 Plus
- Applicant
- Schiller AG
Baar, CH - Received
- December 22, 2006
- Decision date
- March 7, 2007
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DXN – System, Measurement, Blood-Pressure, Non-Invasive
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1130
- Specialty
- Cardiovascular
Other 510(k)s with product code DXN
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261929 | Upper Arm Blood pressure monitor (BP7155D)DXN · Special | OMRON Healthcare, Inc. | 09/10/2026SE |
| K254000 | Happy Health Blood Pressure MonitorDXN · Traditional | Happy Health, Inc. | 09/03/2026SE |
| K262658 | Automatic Digital Blood Pressure monitor (LD-526)DXN · Special | Honsun (Nantong) Co., Ltd. | 08/31/2026SE |
| K261394 | Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-6186 Plus, DBP-6286B Plus…DXN · Traditional | JOYTECH Healthcare Co., Ltd. | 08/26/2026SE |
| K261061 | BP Go (BPP-855)DXN · Traditional | Wellvii, Inc. | 08/13/2026SE |
| K253425 | Arm-type Fully Automatic Digital Blood Pressure Monitor…DXN · Traditional | Joytech Healthcare Co. , Ltd. | 08/13/2026SE |
| K261136 | Blood Pressure Monitor (M501,M501A,M502,M502A,M502C,M502D)DXN · Traditional | Guangzhou Daxin Health Technology Co., Ltd. | 07/23/2026SE |
| K261082 | Microlife Wrist Blood Pressure Monitor , (Model BPHJG5-G)DXN · Traditional | Microlife Corporation | 07/23/2026SE |
| K253126 | Wrist Blood Pressure Monitor (XW-05)DXN · Traditional | Shenzhen Ziqing Medical Equipment Co., Ltd. | 06/18/2026SE |
| K260693 | VicorderCS (VCS-SYS-1100)DXN · Traditional | 80 Beats Medical GmbH | 06/16/2026SE |
More from 80 Beats Medical GmbH
| 510(k) | Device | Decision |
|---|---|---|
| K253562 | medilogFDMWJ · Traditional | 08/14/2026SE |
| K221056 | Argus PB-3000MHX · Traditional | 07/06/2023SE |
| K183425 | Cardiovit AT-102 G2DPS · Traditional | 03/02/2020SE |
| K170182 | Cardiovit FT-1DPS · Traditional | 07/19/2017SE |
| K152043 | Diagnostic Station DS20DPS · Traditional | 05/06/2016SE |
| K101619 | Welch Allyn 1500 Patient MonitorMHX · Traditional | 11/12/2010SE |
| K053207 | Argus, Model LCMMHX · Traditional | 05/19/2006SE |
| K051368 | BR 102 Plus Blood Pressure Holter SystemDXN · Traditional | 08/09/2005SE |
| K050686 | Cardiovit AT-10PLUSDPS · Traditional | 05/04/2005SE |
| K033738 | Monitoring System, Model Argus PB-2200DSK · Traditional | 08/24/2004SE |
Questions and answers
When was BP-200 Plus cleared by the FDA?
BP-200 Plus (K063814) received a 510(k) decision of Substantially Equivalent on March 7, 2007, 75 days after the submission was received.
What is the product code of K063814?
The FDA product code is DXN – System, Measurement, Blood-Pressure, Non-Invasive, a Class II (moderate risk) device regulated under 21 CFR 870.1130.