McKesson 259-SD3V-8
by Mckesson Medical-Surgical Inc.
McKesson 259-SD3V-8 is a Class II device made by Mckesson Medical-Surgical Inc., cleared under FDA 510(k) K140579 on 6 Feb 2015 and listed in FDA GUDID since 16 Jun 2025 (UDI-DI 10612479277165), active as of 23 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 | Number10612479277165 | Date16 Jun 2025 | StatusListed |
| United States | FDA 510(k) | NumberK140579 | Date6 Feb 2015 | StatusActive |
Official records
- AccessGUDID record 10612479277165
- FDA 510(k) database K140579
Across registries
- FDA 510(k) K140579 decided 6 Feb 2015 Active
- FDA GUDID UDI-DI 10612479277165 listed 16 Jun 2025 Listed
Timeline
- Cleared FDA 510(k) K140579
- Listed FDA GUDID 10612479277165
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- McKesson
- Generic name
- Vascular ultrasound system control unit
- Model / reference
- 259-SD3V-8
- Primary DI / UDI-DI
- 10612479277165
- 510(k) Number
- FDA product code
- KNG
- GMDN term
- Vascular ultrasound system control unit
- Device class
- Class II
- Regulation number
- 884.2660
- GUDID distribution status
- In Commercial Distribution
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