Supermon Neonatal Non-Invasive Blood Press. 7283
FDA 510(k) K882955 · Kontron Instruments, Inc.
510(k) numberK882955
Submission
- Device name
- Supermon Neonatal Non-Invasive Blood Press. 7283
- Applicant
- Kontron Instruments, Inc.
Everett, MA, US - Received
- July 14, 1988
- Decision date
- January 26, 1990
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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 |
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| K971038 | Kontron Kolormon Plus ECG with Respiration ModuleDPS · Traditional | 09/24/1997SE |
| K932268 | Modifications to Intra-Aortic BalloonsDSP · Traditional | 12/15/1993SE |
| K925248 | Modification of Intra-Aortic Balloon CathetersDSP · Traditional | 09/27/1993SE |
| K923603 | Intra-Aortic Balloon Pump Catheter - ModificationDYB · Traditional | 03/08/1993SE |
| K905313 | Kontron Intra-Aortic Balloon Pump, Model Kaat IIDSP · Traditional | 06/19/1991SE |
| K903344 | 9.5 FR Percutaneous DB Lumen 40CC Flexi-Cath (TM)DSP · Traditional | 01/15/1991SE |
| K896437 | Kontron Sigma 44 HVCD Ultrasound Imaging SystemDPT · Traditional | 12/03/1990SE |
| K892222 | 9.5F Percu Double Lumen Intra-Aortic BalloonDSP · Traditional | 09/14/1990SE |
| K896386 | Minimon 7133B Patient MonitorDPS · Traditional | 12/13/1989SE |
| K896417 | Kontron Kolormon 7250 Patient MonitorDPS · Traditional | 12/12/1989SE |
Questions and answers
When was Supermon Neonatal Non-Invasive Blood Press. 7283 cleared by the FDA?
Supermon Neonatal Non-Invasive Blood Press. 7283 (K882955) received a 510(k) decision of Substantially Equivalent on January 26, 1990, 561 days after the submission was received.
What is the product code of K882955?
The FDA product code is DXN – System, Measurement, Blood-Pressure, Non-Invasive, a Class II (moderate risk) device regulated under 21 CFR 870.1130.