V20, V20a, AVSM3 SNF
FDA 510(k) K200434 · Mediana Co., Ltd.
510(k) numberK200434
Submission
- Device name
- V20, V20a, AVSM3 SNF
- Applicant
- Mediana Co., Ltd.
Wonju-Si, KR - Received
- February 24, 2020
- Decision date
- October 9, 2020
- 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 |
|---|---|---|
| K170497 | V10DXN · Traditional | 12/15/2017SE |
| K160358 | DT-100FLL · Traditional | 02/24/2017SE |
| K152659 | V10DXN · Traditional | 08/25/2016SE |
| K112190 | Patient MonitorMHX · Traditional | 11/09/2011SE |
| K110612 | FM20HGM · Traditional | 11/08/2011SE |
| K110630 | F10KNG · Traditional | 06/24/2011SE |
| K100225 | Pulse Oximeter Model P10DQA · Traditional | 02/09/2011SE |
| K100217 | Lucon M-Series Patient Monitor, Models M20 and M30MHX · Traditional | 06/08/2010SE |
| K051375 | Vital Signs MonitorDXN · Traditional | 07/28/2005SE |
Questions and answers
When was V20, V20a, AVSM3 SNF cleared by the FDA?
V20, V20a, AVSM3 SNF (K200434) received a 510(k) decision of Substantially Equivalent on October 9, 2020, 228 days after the submission was received.
What is the product code of K200434?
The FDA product code is DXN – System, Measurement, Blood-Pressure, Non-Invasive, a Class II (moderate risk) device regulated under 21 CFR 870.1130.