Hokanson UPC3.3
Hokanson UPC3.3 (03528) 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 9 Sep 2016 (UDI-DI 00817065021020), active (FDA 510(k)), not in commercial distribution (GUDID) 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 | Number00817065021020 | Date9 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK041689 | Date6 Aug 2004 | StatusActive |
Official records
- AccessGUDID record 00817065021020
- FDA 510(k) database K041689
Across registries
- FDA 510(k) K041689 decided 6 Aug 2004 Active
- FDA GUDID UDI-DI 00817065021020 listed 9 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K041689
- Listed FDA GUDID 00817065021020
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- Withdrawn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
- UPC3.3, 03528
- Primary DI / UDI-DI
- 00817065021020
- 510(k) Number
- FDA product code
- DXQ
- GMDN term
- Blood pressure cuff, reusable
- Device class
- Class II
- Regulation number
- 870.1120
- GUDID distribution status
- Not in Commercial Distribution
- Size
- Length — 12 CentimeterWidth — 3.3 Centimeter
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Other devices filed under FDA product code DXQ (Blood Pressure Cuff).
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