FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
Blood Pressure Monitor (B73, BE23T)
K Number: K251331
·
Decision Oct 27, 2025
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
7
Review Days
180
Basic Information
- Device Name
- Blood Pressure Monitor (B73, BE23T)
- K Number
- K251331
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1130
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Shenzhen Jamr Technology Co., Ltd.
- Date Received
- April 30, 2025
- Decision Date
- October 27, 2025
- Product Code
- DXN
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| DXN | System, Measurement, Blood-Pressure, Non-Invasive | FDA class 2 | Cardiovascular |
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Other Clearances by Shenzhen Jamr Technology Co., Ltd.
| K Number | Device Name | ||
|---|---|---|---|
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