LFE — Solution, Cold Sterilizing Class II
FDA product code LFE covers "Solution, Cold Sterilizing", a Class II medical device regulated under 21 CFR 880.6885. Submissions are reviewed by the General Hospital panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- LFE
- Device Class
- Class II
- Regulation Number
- 880.6885
- Submission Type
- Review Panel
- DE
- Medical Specialty
- General Hospital
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K830106 | north pacific dental | UNICIDE | March 7, 1983 |