Hokanson MD6 Doppler probe
Hokanson MD6 Doppler probe (01952) is a Class II device made by D. E. Hokanson, Inc., cleared under FDA 510(k) K901592 on 22 Oct 1990 and listed in FDA GUDID since 16 Sep 2016 (UDI-DI 00817065021464), 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 | Number00817065021464 | Date16 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK901592 | Date22 Oct 1990 | StatusActive |
Official records
- AccessGUDID record 00817065021464
- FDA 510(k) database K901592
Across registries
- FDA 510(k) K901592 decided 22 Oct 1990 Active
- FDA GUDID UDI-DI 00817065021464 listed 16 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K901592
- Listed FDA GUDID 00817065021464
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Hokanson
- Generic name
- Noninvasive vascular ultrasound system probe
- Model / Ref / Catalog
- MD6 Doppler probe, 01952
- Primary DI / UDI-DI
- 00817065021464
- 510(k) Number
- FDA product code
- DXK
- GMDN term
- Noninvasive vascular ultrasound system probe
- Device class
- Class II
- Regulation number
- 870.2330
- GUDID distribution status
- In Commercial Distribution
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