Hokanson 43663
Hokanson 43663 is a Class II device made by D. E. Hokanson, Inc., cleared under FDA 510(k) K041689 on 6 Aug 2004 and listed in FDA GUDID since 12 May 2017 (UDI-DI 00817065021754), 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 | Number00817065021754 | Date12 May 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK041689 | Date6 Aug 2004 | StatusActive |
Official records
- AccessGUDID record 00817065021754
- FDA 510(k) database K041689
Across registries
- FDA 510(k) K041689 decided 6 Aug 2004 Active
- FDA GUDID UDI-DI 00817065021754 listed 12 May 2017 Listed
Timeline
- Cleared FDA 510(k) K041689
- Listed FDA GUDID 00817065021754
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Hokanson
- Generic name
- Blood pressure cuff, reusable
- Model / Ref / Catalog
- 43663
- Primary DI / UDI-DI
- 00817065021754
- 510(k) Number
- FDA product code
- DXQ
- GMDN term
- Blood pressure cuff, reusable
- Device class
- Class II
- Regulation number
- 870.1120
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 12 CentimeterWidth — 2.5 Centimeter
Similar devices in this category
Other devices filed under Blood pressure cuff, reusable.