Vector R&D, Inc ML750
Vector R&D, Inc ML750 is a Class I device made by Vector R&D, Inc., cleared under FDA 510(k) K022535 on 22 Oct 2002 and listed in FDA GUDID since 30 Sep 2022 (UDI-DI 00810113690322), 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 | GUDID listing | Number00810113690322 | Date30 Sep 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK022535 | Date22 Oct 2002 | StatusActive |
Official records
- AccessGUDID record 00810113690322
- FDA 510(k) database K022535
Across registries
- FDA 510(k) K022535 decided 22 Oct 2002 Active
- FDA GUDID UDI-DI 00810113690322 listed 30 Sep 2022 Listed
Timeline
- Cleared FDA 510(k) K022535
- Listed FDA GUDID 00810113690322
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Vector R&D, Inc
- Generic name
- Dental delivery system instrument unit, pneumatic
- Model / Ref / Catalog
- ML750
- Primary DI / UDI-DI
- 00810113690322
- 510(k) Number
- FDA product code
- EFB
- GMDN term
- Dental delivery system instrument unit, pneumatic
- Device class
- Class I
- Regulation number
- 872.4200
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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