FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
RADIAL ARTERY COMPRESSION TOURNIQUET
K Number: K111837
·
Decision Sep 27, 2011
Classifications
1
FEI Numbers
186
Registration Numbers
186
Same Product Code
203
Applicant Total
7
Review Days
90
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Basic Information
- Device Name
- RADIAL ARTERY COMPRESSION TOURNIQUET
- K Number
- K111837
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.4450
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Lepu Medical Technology (Beijing) Co., Ltd.
- Date Received
- June 29, 2011
- Decision Date
- September 27, 2011
- Product Code
- DXC
- 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 |
|---|---|---|---|
| DXC | Clamp, Vascular | FDA class 2 | Cardiovascular |
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