Low & High Speed Kit
by Dpm USA Corp
510(k) K090055
Low & High Speed Kit is a Class I device made by Dpm USA Corp, cleared under FDA 510(k) K090055 on 27 Oct 2009, active as of 9 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK090055 | Date27 Oct 2009 | StatusActive |
Official records
- FDA 510(k) database K090055
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- EFA
- FDA applicant
- Dpm USA Corp.
- Device class
- Class I
- Regulation
- 21 CFR Part 872.4200
- Advisory committee
- Dental
- FDA decision
- SESE Substantially Equivalent
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