Jetstream
by Deldent Ltd.
510(k) K014252
Jetstream is a medical device (FDA Class II; FDA product code KOJ, Airbrush) made by Deldent Ltd., cleared under FDA 510(k) K014252 on 19 Feb 2002, active as of 22 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 | NumberK014252 | Date19 Feb 2002 | StatusActive |
Official records
- FDA 510(k) database K014252
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- KOJ
- FDA applicant
- Deldent , Ltd.
- Device class
- Class II
- Regulation
- 21 CFR Part 872.6080
- Advisory committee
- Dental
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K014252
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| JETSTREAM 115 V | 506300 / 115 V | 07290016281842 | — | On the market |
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