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Hokanson RD2™

by D. E. Hokanson, Inc.

Hokanson RD2™ (03599) is a Class II device made by D. E. Hokanson, Inc., cleared under FDA 510(k) K842067 on 1 Mar 1985 and listed in FDA GUDID since 31 Aug 2017 (UDI-DI 00817065022386), 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) K842067

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 Number00817065022386 UDI-DI Date31 Aug 2017ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK842067 Date1 Mar 1985DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K842067 decided 1 Mar 1985 Active
  • FDA GUDID UDI-DI 00817065022386 listed 31 Aug 2017 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K842067
  2. Listed FDA GUDID 00817065022386

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  • Withdrawn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 deflator
Model / Ref / Catalog
RD2™, 03599
Primary DI / UDI-DI
00817065022386
510(k) Number
FDA product code
DXN
GMDN term
Blood pressure cuff deflator
Device class
Class II
Regulation number
870.1130
GUDID distribution status
In Commercial Distribution

Related devices

Category: Blood pressure cuff deflator

Cleared under the same submission (K842067)

Similar devices

Other devices filed under FDA product code DXN (System, Measurement, Blood-Pressure, Non-Invasive).

Other devices from D. E. Hokanson, Inc.

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

Properties

  • Manufacturing date
Other properties (14, all answered No)