FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
Huber Needle Infusion Set, Safety Huber Needle Infusion Set
K Number: K200463
·
Decision Apr 7, 2021
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
12
Applicant Total
15
Review Days
407
Basic Information
- Device Name
- Huber Needle Infusion Set, Safety Huber Needle Infusion Set
- K Number
- K200463
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5570
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Jiangsu Caina Medical Co.,Ltd
- Date Received
- February 25, 2020
- Decision Date
- April 7, 2021
- Product Code
- PTI
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| PTI | Non-Coring (Huber) Needle | FDA class 2 | General Hospital |
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