Rebox (Uk) , Ltd.

Rebox (Uk) , Ltd. holds 1 FDA 510(k) medical device clearance, cleared in 1990.

Top product codes for Rebox (Uk) , Ltd.

GZJ — Neurology1 device

Recent clearances by Rebox (Uk) , Ltd.

K895183 — REBOX II (TENS)Code GZJ·1990-01-19

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