FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
REDON SET
K Number: K001716
·
Decision Jul 19, 2000
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
76
Applicant Total
3
Review Days
44
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Basic Information
- Device Name
- REDON SET
- K Number
- K001716
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4780
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Pfm Produkte Fur Die Medizin AG
- Date Received
- June 5, 2000
- Decision Date
- July 19, 2000
- Product Code
- JCX
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| JCX | Apparatus, Suction, Ward Use, Portable, Ac-Powered | FDA class 2 | General, Plastic Surgery |
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