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Hokanson 03620

by D. E. Hokanson, Inc.

Hokanson 03620 is a Class II device made by D. E. Hokanson, Inc., listed in FDA GUDID since 9 Sep 2016 (UDI-DI 00817065020023), not in commercial distribution (GUDID) as of 22 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00817065020023 UDI-DI Date9 Sep 2016ListedStatusListed GUDID: not in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Hokanson
Generic name
Blood pressure cuff, reusable
Model / Ref / Catalog
03620
Primary DI / UDI-DI
00817065020023
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
Width — 10 Centimeter

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

  • Premarket exempt
  • Manufacturing date
Other properties (13, all answered No)