FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
LIGACLIP 20/20* MULTIPLE CLIP APPLIER
K Number: K864102
·
Decision Nov 5, 1986
Classifications
1
FEI Numbers
110
Registration Numbers
110
Same Product Code
172
Applicant Total
172
Review Days
15
Basic Information
- Device Name
- LIGACLIP 20/20* MULTIPLE CLIP APPLIER
- K Number
- K864102
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4300
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- ETHICON, INC.
- Date Received
- October 21, 1986
- Decision Date
- November 5, 1986
- Product Code
- FZP
- 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 |
|---|---|---|---|
| FZP | Clip, Implantable | FDA class 2 | General, Plastic Surgery |
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