FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
LAFACI
K Number: K032400
·
Decision May 7, 2004
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
74
Applicant Total
1
Review Days
277
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Basic Information
- Device Name
- LAFACI
- K Number
- K032400
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.5070
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Vision Pro, LLC
- Date Received
- August 4, 2003
- Decision Date
- May 7, 2004
- Product Code
- FYD
- Advisory Committee
- General, Plastic Surgery
- 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 |
|---|---|---|---|
| FYD | Apparatus, Exhaust, Surgical | FDA class 2 | General, Plastic Surgery |
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