FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇹 Italy
Pentaflush
K Number: K214080
·
Decision Jul 20, 2022
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
39
Applicant Total
3
Review Days
205
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Basic Information
- Device Name
- Pentaflush
- K Number
- K214080
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5200
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Pentaferte Italia S.R.L.
- Date Received
- December 27, 2021
- Decision Date
- July 20, 2022
- Product Code
- NGT
- 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 |
|---|---|---|---|
| NGT | Saline, Vascular Access Flush | FDA class 2 | General Hospital |
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