FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
BAND-AID BRAND TRICOT MESH BANDAGES
K Number: K801823
·
Decision Aug 20, 1980
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
5
Applicant Total
206
Review Days
20
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Basic Information
- Device Name
- BAND-AID BRAND TRICOT MESH BANDAGES
- K Number
- K801823
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4100
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Applicant
- Johnson & Johnson Professionals, Inc.
- Date Received
- July 31, 1980
- Decision Date
- August 20, 1980
- Product Code
- KGY
- 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 |
|---|---|---|---|
| KGY | Bag, Intestine | FDA class 1 | General, Plastic Surgery |
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