FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ALGINATE FIBER
K Number: K914779
·
Decision Dec 4, 1991
Classifications
1
FEI Numbers
500
Registration Numbers
500
Same Product Code
3
Applicant Total
3
Review Days
42
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Basic Information
- Device Name
- ALGINATE FIBER
- K Number
- K914779
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4018
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Adri/Technam
- Date Received
- October 23, 1991
- Decision Date
- December 4, 1991
- Product Code
- NAC
- 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 |
|---|---|---|---|
| NAC | Dressing, Wound, Hydrophilic | FDA class 1 | General, Plastic Surgery |
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