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Hokanson 03840

by D. E. Hokanson, Inc.

Hokanson 03840 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 27 Mar 2026 (UDI-DI 00817065022652), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K041689

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00817065022652 UDI-DI Date27 Mar 2026ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Special NumberK041689 Date6 Aug 2004DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K041689 decided 6 Aug 2004 Active
  • FDA GUDID UDI-DI 00817065022652 listed 27 Mar 2026 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K041689
  2. Listed FDA GUDID 00817065022652

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Hokanson
Generic name
Blood pressure cuff, reusable
Model / Ref / Catalog
03840
Primary DI / UDI-DI
00817065022652
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
Width — 1.9 Centimeter
Length — 9 Centimeter

Related devices

Cleared under the same submission (K041689)

and 8 more cleared under K041689

Similar devices

Other devices filed under FDA product code DXQ (Blood Pressure Cuff).

Other devices from D. E. Hokanson, Inc.

See all devices from D. E. Hokanson, Inc. →

Properties

  • Lot / batch number
  • Manufacturing date
Other properties (13, all answered No)