Drfp Prosmart Root Canal Obturation System, Propoints 4% 6%, Pt, S
by Drfp, Ltd. 510(k)
Active
510(k) K100248
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK100248 | Date22 Oct 2010 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- KIF
- FDA applicant
- Drfp , Ltd.
- Device Class
- Class II
- Regulation
- 21 CFR Part 872.3820
- Advisory Committee
- Dental
- FDA Decision
- SESE Substantially Equivalent