FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BLOOD PRESSURE RECORDER
K Number: K781932
·
Decision Nov 29, 1978
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
3
Review Days
9
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Basic Information
- Device Name
- BLOOD PRESSURE RECORDER
- K Number
- K781932
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1130
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Cardiodyne, Inc.
- Date Received
- November 20, 1978
- Decision Date
- November 29, 1978
- 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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