KGT — Drape, Adhesive, Aerosol Class I
FDA product code KGT covers "Drape, Adhesive, Aerosol", a Class I medical device regulated under 21 CFR 878.4380. Submissions are reviewed by the General, Plastic Surgery panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- KGT
- Device Class
- Class I
- Regulation Number
- 878.4380
- Submission Type
- Review Panel
- HO
- Medical Specialty
- General, Plastic Surgery
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K851612 | mowbray co | DERMA PREP | May 3, 1985 |