Star Dental 430 Series High Speed Handpiece
510(k) K960719
Active
510(k)
Valid until
No expiry
FDA recalls
None ongoingDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK960719 | Date28 Mar 1996 | StatusActive |
Recalls
-
- Terminated Z-0313-2007
End cap component can disassemble.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- EFA
- Device Class
- Class I
- Regulation
- 21 CFR Part 872.4200
- Advisory Committee
- Dental
- FDA Decision
- SESE Substantially Equivalent