Hi-Dow International, Inc.

Hi-Dow International, Inc. holds 6 FDA 510(k) medical device clearances, first cleared 2011, most recent 2024.

Top product codes for Hi-Dow International, Inc.

Recent clearances by Hi-Dow International, Inc.

K233461 — Hi-Dow PRO TOUCH WIRELESS 6-12 (HD-19A)Code NUH·2024-01-19
K210383 — Wrap Accessory ElectrodesCode GXY·2021-11-12
K202337 — Pulsed electromagnetic field wrapCode ILX·2020-12-15
K190617 — Wrap accessory electrodesCode GXY·2019-07-02
K163393 — Hi-Dow Wireless TENS/EMS System (Model HD-5N)Code NUH·2017-08-04
K102598 — HI-DOW-XPCode NUH·2011-05-13

Data sourced from openFDA. This site is unofficial and independent of the FDA.