FDA 510(k)
FDA class 1
Substantially Equivalent for Some Indications
🇺🇸 United States
DERMATEC TRANSPARENT FILM DRESSING
K Number: K863580
·
Decision Dec 31, 1986
Classifications
1
FEI Numbers
502
Registration Numbers
502
Same Product Code
106
Applicant Total
4
Review Days
125
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Basic Information
- Device Name
- DERMATEC TRANSPARENT FILM DRESSING
- K Number
- K863580
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 878.4020
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent for Some Indications
- Applicant
- Dermatec, Inc.
- Date Received
- August 28, 1986
- Decision Date
- December 31, 1986
- Product Code
- NAD
- 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 |
|---|---|---|---|
| NAD | Dressing, Wound, Occlusive | FDA class 1 | General, Plastic Surgery |
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