FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BP-BT Kiosk
K Number: K200287
·
Decision May 15, 2020
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
14
Review Days
100
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Basic Information
- Device Name
- BP-BT Kiosk
- K Number
- K200287
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1130
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Ld Technology, LLC
- Date Received
- February 5, 2020
- Decision Date
- May 15, 2020
- 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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| K131568 | SUDO PATH | Jun 28, 2013 | Substantially Equivalent |
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| K113264 | ELECTRO SENSOR COMPLEX SOFTWARE (ES COMPLEX SOFTWARE) | Mar 2, 2012 | Substantially Equivalent |
| K103026 | ELECTRO SENSOR -BODY COMPOSITION | Mar 29, 2011 | Substantially Equivalent |