FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇱 Israel
EXTENTION SET
K Number: K933524
·
Decision May 23, 1995
Classifications
1
FEI Numbers
66
Registration Numbers
66
Same Product Code
63
Applicant Total
4
Review Days
672
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Basic Information
- Device Name
- EXTENTION SET
- K Number
- K933524
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5440
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Mediziv Medical Products 1987 , Ltd.
- Date Received
- July 20, 1993
- Decision Date
- May 23, 1995
- Product Code
- FPK
- 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 |
|---|---|---|---|
| FPK | Tubing, Fluid Delivery | FDA class 2 | General Hospital |
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