Hokanson 5.40
by D. E. Hokanson, Inc. 7 variants
Hokanson 5.40 (03413) is a Class II device made by D. E. Hokanson, Inc., cleared under FDA 510(k) K970570 on 3 Oct 1997 and listed in FDA GUDID since 16 Sep 2016 (UDI-DI 00817065021150), 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 | Number00817065021150 | Date16 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK970570 | Date3 Oct 1997 | StatusActive |
Official records
- AccessGUDID record 00817065021150
- FDA 510(k) database K970570
Across registries
- FDA 510(k) K970570 decided 3 Oct 1997 Active
- FDA GUDID UDI-DI 00817065021150 listed 16 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K970570
- Listed FDA GUDID 00817065021150
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Hokanson
- Generic name
- Peripheral vascular haemodynamic measurement application software
- Model / Ref / Catalog
- 5.40, 03413
- Primary DI / UDI-DI
- 00817065021150
- 510(k) Number
- FDA product code
- DQK
- GMDN term
- Peripheral vascular haemodynamic measurement application software
- Device class
- Class II
- Regulation number
- 870.1425
- GUDID distribution status
- In Commercial Distribution
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