FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer
K Number: K193259
·
Decision Jul 2, 2020
Classifications
1
FEI Numbers
172
Registration Numbers
172
Same Product Code
197
Applicant Total
3
Review Days
219
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Basic Information
- Device Name
- Aneroid sphygmomanometer with stethoscope, Aneroid sphygmomanometer
- K Number
- K193259
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1120
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Little Doctor Electronic (Nantong)Co.,Ltd
- Date Received
- November 26, 2019
- Decision Date
- July 2, 2020
- Product Code
- DXQ
- 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 |
|---|---|---|---|
| DXQ | Blood Pressure Cuff | FDA class 2 | Cardiovascular |
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