DS-240 Ambulatory Blood Pressure Monitoring System
FDA 510(k) K913595 · Koven and Assoc., Inc.
510(k) numberK913595
Submission
- Device name
- DS-240 Ambulatory Blood Pressure Monitoring System
- Applicant
- Koven and Assoc., Inc.
St. Louis, MO, US - Received
- August 13, 1991
- Decision date
- March 27, 1992
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement 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 |
|---|---|---|
| K922669 | Multidop Model HD-2020 Bi-Directional Blood FlowDPW · Traditional | 01/29/1993SE |
| K920333 | Smartdop 20 Bi-Directional Blood Flow DetectorDPW · Traditional | 01/22/1993SE |
| K915550 | Mini Doppler II Ultrasound Blood Flow DetectorDPW · Traditional | 12/10/1992SE |
| K912409 | Model HD-207 Bidirectional Velocity MeterJOP · Traditional | 12/23/1991SE |
| K903026 | ES-1000SP II Smart DopDPW · Traditional | 02/26/1991SE |
| K894892 | HD-2200 Pneumo-Dop Vascular Testing SystemDSB · Traditional | 10/27/1989SE |
| K892707 | DVM-4200 Blood FlowmeterDPW · Traditional | 07/28/1989SE |
Questions and answers
When was DS-240 Ambulatory Blood Pressure Monitoring System cleared by the FDA?
DS-240 Ambulatory Blood Pressure Monitoring System (K913595) received a 510(k) decision of Substantially Equivalent on March 27, 1992, 227 days after the submission was received.
What is the product code of K913595?
The FDA product code is DXN – System, Measurement, Blood-Pressure, Non-Invasive, a Class II (moderate risk) device regulated under 21 CFR 870.1130.